Dbfetch
ID MN003302; SV 1; linear; genomic DNA; STD; HUM; 2710 BP. XX AC MN003302; XX DT 27-FEB-2020 (Rel. 143, Created) DT 27-FEB-2020 (Rel. 143, Last updated, Version 1) XX DE Homo sapiens clone B_112399_06638 MHC class I antigen (HLA-B) gene, 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 XX RN [1] RP 1-2710 RA Cereb N., Yang S.Y.; RT "HLA new alleles found by Histogenetics"; RL Unpublished. XX RN [2] RP 1-2710 RA Cereb N., Yang S.Y.; RT ; RL Submitted (31-MAY-2019) to the INSDC. RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA XX DR MD5; 30b64ea566e497bafc64597bb47c6355. XX FH Key Location/Qualifiers FH FT source 1..2710 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /clone="B_112399_06638" FT /db_xref="taxon:9606" FT gene 1..>2710 FT /gene="HLA-B" FT mRNA join(1..109,238..507,754..1029,1601..1876,1970..2086, FT 2528..2560,2667..>2710) FT /gene="HLA-B" FT /product="MHC class I antigen" FT exon 1..109 FT /gene="HLA-B" FT /number=1 FT 5'UTR 1..36 FT /gene="HLA-B" FT CDS join(37..109,238..507,754..1029,1601..1876,1970..2086, FT 2528..2560,2667..2710) FT /codon_start=1 FT /gene="HLA-B" FT /product="MHC class I antigen" FT /protein_id="QDK62830.1" FT /translation="MLVMAPRTVLLLLSAALALTETWAGSHSMRYFYTSVSRPGRGEPR FT FISVGYVDDTQFVRFDSDAASPREEPRAPWIEQEGPEYWDRNTQICKTNTQTDRESLRN FT LRGYYNQSEAGSHTLQWMYGCDVGPDGRLLRGYNQFAYDGKDYIALNEDLSSWTAADTA FT AQITQRKWEAAREAEQLRAYLEGTCVEWLRRHLENGKETLQRADPPKTHVTHHPISDHE FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY FT TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK FT GGSYSQAASSDSAQGSDVSLTA" FT intron 110..237 FT /gene="HLA-B" FT /number=1 FT exon 238..507 FT /gene="HLA-B" FT /number=2 FT intron 508..753 FT /gene="HLA-B" FT /number=2 FT exon 754..1029 FT /gene="HLA-B" FT /number=3 FT intron 1030..1600 FT /gene="HLA-B" FT /number=3 FT exon 1601..1876 FT /gene="HLA-B" FT /number=4 FT intron 1877..1969 FT /gene="HLA-B" FT /number=4 FT exon 1970..2086 FT /gene="HLA-B" FT /number=5 FT intron 2087..2527 FT /gene="HLA-B" FT /number=5 FT exon 2528..2560 FT /gene="HLA-B" FT /number=6 FT intron 2561..2666 FT /gene="HLA-B" FT /number=6 FT exon 2667..>2710 FT /gene="HLA-B" FT /number=7 XX SQ Sequence 2710 BP; 508 A; 807 C; 855 G; 540 T; 0 other; cacccacccg gactcagagt ctcctcagac gccaagatgc tggtcatggc gccccgaacc 60 gtcctcctgc tgctctcggc ggccctggcc ctgaccgaga cctgggccgg tgagtgcggg 120 tcgggaggga aatggcctct gccgggagga gcgaggggac cgcaggcggg ggcgcaggac 180 ctgaggagcc gcgccgggag gagggtcggg cgggtttcag cccctcctcg cccccaggct 240 cccactccat gaggtatttc tacacctccg tgtcccggcc cggccgcggg gagccccgct 300 tcatctcagt gggctacgtg gacgacacgc agttcgtgag gttcgacagc gacgccgcga 360 gtccgagaga ggagccgcgg gcgccgtgga tagagcagga ggggccggaa tattgggacc 420 ggaacacaca gatctgcaag accaacacac agactgaccg agagagcctg cggaacctgc 480 gcggctacta caaccagagc gaggccggtg agtgaccccg gcccggggcg caggtcacga 540 ctccccatcc cccacggacg gcccgggtcg ccccgagtct ccgggtccga gatccgcctc 600 cctgaggccg cgggacccgc ccagaccctc gaccggcgag agccccaggc gcgtttaccc 660 ggtttcattt tcagttgagg ccaaaatccc cgcgggttgg tcggggcggg gcggggctcg 720 gggggactgg gctgaccgcg ggggcggggc cagggtctca caccctccag tggatgtatg 780 gctgcgacgt ggggccggac gggcgcctcc tccgcgggta taaccagttc gcctacgacg 840 gcaaggatta catcgccctg aacgaggacc tgagctcctg gaccgcggcg gacaccgcgg 900 ctcagatcac ccagcgcaag tgggaggcgg cccgtgaggc ggagcagctg agagcctacc 960 tggagggcac gtgcgtggag tggctccgca gacacctgga gaacgggaag gagacgctgc 1020 agcgcgcggg taccggggca gtggggagcc ttccccatct cctataggtc gccggggatg 1080 gcctcccacg agaagaagag gaaaatggga tcagcgctag aatgtcgccc tcccttgaat 1140 ggagaatggc atgagttttc ctgagtttcc tctgagggcc ccctcttctc tctaggacaa 1200 ttaagggatg acgtctctga ggaaatggag gggaagacag tccctagaat actgatcagg 1260 ggtccccttt gacccctgca gcagccttgg gaaccatgac ttttcttctc aggccttgtt 1320 ctctgcctca cactcagtgt gtttggggct ctgattccag cacttctgag tcactttacc 1380 tccactcaga tcaggagcag aagtctctgt tccccgctca gagactcgaa ctttccaatg 1440 aatagattat cccaggtgcc tgcgtccagg ctggtgtctg ggttctgtgt cccttcccca 1500 ccccaggtgt cctgtccatt ctcaggctgg tcacatgggt ggtcctaggg tgtcccatga 1560 gagatgcaaa gcgcctgaat tttctgactc ttcccatcag accccccaaa gacacatgtg 1620 acccaccacc ccatctctga ccatgaggcc accctgaggt gctgggccct gggcttctac 1680 cctgcggaga tcacactgac ctggcagcgg gatggcgagg accaaactca ggacaccgag 1740 cttgtggaga ccagaccagc aggagacaga accttccaga agtgggcagc tgtggtggtg 1800 ccttctggag aagagcagag atacacatgc catgtacagc atgaggggct gccgaagccc 1860 ctcaccctga gatggggtaa ggagggggat gaggggtcat atctcttctc agggaaagca 1920 ggagcccttc agcagggtca gggcccctca tcttcccctc ctttcccaga gccatcttcc 1980 cagtccaccg tccccatcgt gggcattgtt gctggcctgg ctgtcctagc agttgtggtc 2040 atcggagctg tggtcgctgc tgtgatgtgt aggaggaaga gttcaggtag ggaaggggtg 2100 aggggtgggg tctgggtttt cttgtcccac tgggggtttc aagccccagg tagaagtgtt 2160 ccctgcatca ttactgggaa gcagcatgca cacaggggct aacgcagcct gggaccctgt 2220 gtgccagcac ttactctttt gtgcagcaca tgtgacaatg aaggacggat gtatcacctt 2280 gatggttgtg gtgttggggt cctgattcca gcattcatga gtcaggggaa ggtccctgct 2340 aaggacagac cttaggaggg cagttggtcc aggacccaca cttgctttcc tcgtgtttcc 2400 tgatcctgcc ctgggtctgt agtcatactt ctggaaattc cttttgggtc caagactagg 2460 aggttcctct aagatctcat ggccctgctt cctcccagtc ccctcacagg acattttctt 2520 cccacaggtg gaaaaggagg gagctactct caggctgcgt gtaagtggtg ggggtgggag 2580 tgtggaggag ctcacccacc ccataattcc tcctgtccca cgtctcctgt gggctctgac 2640 caggtcctgt ttttgttcta ctccagccag cgacagtgcc cagggctctg atgtgtctct 2700 cacagcttga 2710 //