Dbfetch

ID   MZ288697; SV 1; linear; genomic DNA; STD; HUM; 3982 BP.
XX
AC   MZ288697;
XX
DT   09-AUG-2022 (Rel. 144, Created)
DT   10-AUG-2022 (Rel. 144, Last updated, Version 1)
XX
DE   Homo sapiens MHC class I antigen (HLA-B) gene, HLA-B*40:491 allele,
DE   complete cds.
XX
KW   .
XX
OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
XX
RN   [1]
RP   1-3982
RA   Kwok J.S.Y., Cheung S.K.F., Ho J.C.Y., Chan Y.;
RT   ;
RL   Submitted (19-MAY-2021) to the INSDC.
RL   Division of Transplantation and Immunogenetics, Department of Pathology,
RL   Queen Mary Hospital, 102 Pokfulam Road, Pokfulam, Hong Kong HKG, Hksar
XX
DR   MD5; 2d63552d71823abdc35fca03b7775680.
XX
CC   ##Assembly-Data-START##
CC   Assembly Method       :: NGSengine v. 2.20.0; TypeStream Visual v.
CC   2.0.1
CC   Sequencing Technology :: Illumina
CC   ##Assembly-Data-END##
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..3982
FT                   /organism="Homo sapiens"
FT                   /mol_type="genomic DNA"
FT                   /db_xref="taxon:9606"
FT   gene            <1..>3982
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT   exon            <1..357
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=1
FT   5'UTR           <1..284
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT   CDS             join(285..357,486..755,1001..1276,1851..2126,2220..2336,
FT                   2778..2810,2917..2960)
FT                   /codon_start=1
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /product="MHC class I antigen"
FT                   /protein_id="UUJ35597.1"
FT                   /translation="MRVTAPRTVLLLLSAALALTETWAGSHSMRYFHTAMSRPGRGEPR
FT                   FITVGCVDDTLFVRFDSDATSPRKEPRAPWIEQEGPEYWDRETQISKTNTQTYRESLRN
FT                   LRGYYNQSEAGSHTLQRMYGCDVGPDGRLLRGHNQYAYDGKDYIALNEDLRSWTAADTA
FT                   AQISQRKLEAARVAEQLRAYLEGECVEWLRRYLENGKDKLERADPPKTHVTHHPISDHE
FT                   ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY
FT                   TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK
FT                   GGSYSQAACSDSAQGSDVSLTA"
FT   intron          358..485
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=1
FT   exon            486..755
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=2
FT   intron          756..1000
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=2
FT   exon            1001..1276
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=3
FT   intron          1277..1850
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=3
FT   exon            1851..2126
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=4
FT   intron          2127..2219
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=4
FT   exon            2220..2336
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=5
FT   intron          2337..2777
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=5
FT   exon            2778..2810
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=6
FT   intron          2811..2916
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=6
FT   exon            2917..>3982
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
FT                   /number=7
FT   3'UTR           2961..>3982
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40:491"
XX
SQ   Sequence 3982 BP; 749 A; 1129 C; 1206 G; 898 T; 0 other;
     gatcaggacg aagtcccagg ccccgggcgg ggctctcagg gtctcaggct ccgagggccg        60
     cgtctgcaat ggggaggcgc agcgttgggg attccccact cccacgagtt tcacttcttc       120
     tcccaaccta tgtcgggtcc ttcttccagg atactcgtga cgcgtcccca tttcccactc       180
     ccattgggtg tcgggtgtct agagaagcca atcagcgtcg ccgtggtccc agttctaaag       240
     tccccacgca cccacccgga ctcagaatct cctcagacgc cgagatgcgg gtcacggcac       300
     cccgaaccgt cctcctgctg ctctcggcgg ccctggccct gaccgagacc tgggccggtg       360
     agtgcgggtc ggcagggaaa tggcctctgt ggggaggagc gaggggaccg caggcggggg       420
     cgcaggaccc ggggagccgc gccgggagga gggtcgggcg ggtctcagct cctcctcgcc       480
     cccaggctcc cactccatga ggtatttcca caccgccatg tcccggcccg gccgcgggga       540
     gccccgcttc atcaccgtgg gctgcgtgga cgacacgctg ttcgtgaggt tcgacagcga       600
     cgccacgagt ccgaggaagg agccgcgggc gccatggata gagcaggagg ggccggagta       660
     ttgggaccgg gagacacaga tctccaagac caacacacag acttaccgag agagcctgcg       720
     gaacctgcgc ggctactaca accagagcga ggccggtgag tgaccccggc ccggggcgca       780
     ggtcacgact ccccatcccc cacgtacggc ccgggtcgcc ccgagtctcc gggtccgaga       840
     tccgaccccc tgaggccgcg ggacccgccc agaccctcga ccggcgagag ccccaggcgc       900
     gtttacccgg tttcattttc agttgaggcc aaaatccccg cgggttggtc ggggcggggc       960
     ggggctcggg ggactgggct gaccgcgggg ccggggccag ggtctcacac cctccagagg      1020
     atgtacggct gcgacgtggg gccggacggg cgcctcctcc gcgggcataa ccagtacgcc      1080
     tacgacggca aggattacat cgccctgaac gaggacctgc gctcctggac cgccgcggac      1140
     acggcggctc agatctccca gcgcaagttg gaggcggccc gtgtggcgga gcagctgaga      1200
     gcctacctgg agggcgagtg cgtggagtgg ctccgcagat acctggagaa cgggaaggac      1260
     aagctggagc gcgctggtac caggggcagt ggggagcctt ccccatctcc tataggtcgc      1320
     cggggatggc ctcccacgag aagaggagga aaatgggatc agcgctagaa tgtcgccctc      1380
     cgttgaatgg agaatggcat gagttttcct gagtttcctc tgagggcccc ctcttctctc      1440
     tagacaatta aggaatgacg tctctgagga aatggagggg aagacagtcc ctagaatact      1500
     gatcaggggt cccctttgac ccctgcagca gccttgggaa ccgtgacttt tcctctcagg      1560
     ccttgttctc tgcctcacac tcagtgtgtt tggggctctg attccagcac ttctgagtca      1620
     ctttacctcc actcagatca ggagcagaag tccctgttcc ccgctcagag actcgaactt      1680
     tccaatgaat aggagattat cccaggtgcc tgcgtccagg ctggtgtctg ggttctgtgc      1740
     cccttcccca ccccaggtgt cctgtccatt ctcaggctgg tcacatgggt ggtcctaggg      1800
     tgtcccatga aagatgcaaa gcgcctgaat tttctgactc ttcccatcag accccccaaa      1860
     gacacacgtg acccaccacc ccatctctga ccatgaggcc accctgaggt gctgggccct      1920
     gggtttctac cctgcggaga tcacactgac ctggcagcgg gatggcgagg accaaactca      1980
     ggacactgag cttgtggaga ccagaccagc aggagataga accttccaga agtgggcagc      2040
     tgtggtggtg ccttctggag aagagcagag atacacatgc catgtacagc atgaggggct      2100
     gccgaagccc ctcaccctga gatggggtaa ggagggggat gaggggtcat atctcttctc      2160
     agggaaagca ggagcccttc agcagggtca gggcccctca tcttcccctc ctttcccaga      2220
     gccgtcttcc cagtccaccg tccccatcgt gggcattgtt gctggcctgg ctgtcctagc      2280
     agttgtggtc atcggagctg tggtcgctgc tgtgatgtgt aggaggaaga gttcaggtag      2340
     ggaaggggtg aggggtgggg tctgggtttt cttgtcccac tgggggtttc aagccccagg      2400
     tagaagtgtt ccctgcctca ttactgggaa gcagcatgca cacaggggct aacgcagcct      2460
     gggaccctgt gtgccagcac ttactctttt gtgcagcaca tgtgacaatg aaggatggat      2520
     gtatcacctt gatggttgtg gtgttggggt cctgattcca gcattcatga gtcaggggaa      2580
     ggtccctgct aaggacagac cttaggaggg cagttggtcc aggacccaca cttgctttcc      2640
     tcgtgtttcc tgatcctgcc ctgggtctgt agtcatactt ctggaaattc cttttgggtc      2700
     caagactagg aggttcctct aagatctcat ggccctgctt cctcccagtg ccctcacagg      2760
     acattttctt cccacaggtg gaaaaggagg gagctactct caggctgcgt gtaagtggtg      2820
     ggggtgggag tgtggaggag ctcacccacc ccataattcc tcctgtccca cgtctcctgc      2880
     gggctctgac caggtcctgt ttttgttcta ctccaggcag cgacagtgcc cagggctctg      2940
     atgtgtctct cacagcttga aaaggtgaga ttcttggggt ctagagtggg tggggtggcg      3000
     ggtctggggg tgggtggggc agaggggaaa ggcctgggta atggggattc tttgattggg      3060
     atgtttcgcg tgtgtggtgg gctgtttaga gtgtcatcgc ttaccatgac taaccagaat      3120
     ttgttcatga ctgttgtttt ctgtagcctg agacagctgt cttgtgaggg actgagatgc      3180
     aggatttctt cacgcctccc ctttgtgact tcaagagcct ctggcatctc tttctgcaaa      3240
     ggcacctgaa tgtgtctgcg tccctgttag cataatgtga ggaggtggag agacagccca      3300
     cccttgtgtc cactgtgacc cctgttccca tgctgacctg tgtttcctcc ccagtcatct      3360
     ttcttgttcc agagaggtgg ggctggatgt ctccatctct gtctcaactt tacgtgcact      3420
     gagctgcaac ttcttacttc cctactgaaa ataagaatct gaatataaat ttgttttctc      3480
     aaatatttgc tatgagaggt tgatggatta attaaataag tcaattcctg gaatttgaaa      3540
     gagcaaataa agacctgaga accttccaga atctgcatgt tcgctgtgct gagtctgttg      3600
     caggtggggt gtggagaagg ctgtgggggg ccgagtgtgg atggggcctg tgcccatttg      3660
     gtgttgagtc catcatgggc tttatgtggt tagtcctcag ctgggtcacc ttcactgctc      3720
     cattgtcctt gtcccttcag tggaaacttg tccagcggga gctgtgacca cagaggctca      3780
     cacatcgccc agggcggccc ctgcacacgg ggatctctgt gcattctgag acaaattttc      3840
     agagccattc acctcctgcc ctgcttctag agctcctttt ctgctctgct cttctgccct      3900
     ctctccctgc cctggttcta gtgatcttgg tgctgaatcc aatcccaact catgaatctg      3960
     taaagcagag tctaatttag ac                                               3982
//