Dbfetch
ID MK704504; SV 1; linear; genomic DNA; STD; HUM; 2980 BP. XX AC MK704504; XX DT 16-JUL-2019 (Rel. 141, Created) DT 16-JUL-2019 (Rel. 141, Last updated, Version 1) XX DE Homo sapiens MHC class I antigen (HLA-B) gene, 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 1-2980 RA Kleiser M.M.K., Spinnler R.R.S.; RT ; RL Submitted (27-MAR-2019) to the INSDC. RL HLA-Labor, Universityhospital Basel, Petersgraben 4, Basel, Basel-Stadt RL 4031, Switzerland XX DR MD5; 5007913fbd5a72c56d177cb9c60e14b7. XX CC ##Assembly-Data-START## CC Assembly Method :: NGSengine v. 2.12.0.12130 CC Sequencing Technology :: Illumina CC ##Assembly-Data-END## XX FH Key Location/Qualifiers FH FT source 1..2980 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /db_xref="taxon:9606" FT gene <1..>2980 FT /gene="HLA-B" FT mRNA join(<1..348,477..746,993..1268,1841..2116,2210..2326, FT 2768..2800,2907..>2980) FT /gene="HLA-B" FT /product="MHC class I antigen" FT exon <1..348 FT /gene="HLA-B" FT /allele="B*08var" FT /number=1 FT 5'UTR <1..275 FT /gene="HLA-B" FT /allele="B*08var" FT CDS join(276..348,477..746,993..1268,1841..2116,2210..2326, FT 2768..2800,2907..2950) FT /codon_start=1 FT /gene="HLA-B" FT /allele="B*08var" FT /product="MHC class I antigen" FT /protein_id="QDJ94078.1" FT /translation="MLVMAPRTVLLLLSAALALTETWAASHSMRYFDTAMSRPGRGEPR FT FISVGYVDDTQFVRFDSDAASPREEPRAPWIEQEGPEYWDRNTQIFKTNTQTDRESLRN FT LRGYYNQSEAGSHTLQSMYGCDVGPDGRLLRGHNQYAYDGKDYIALNEDLRSWTAADTA FT AQITQRKWEAARVAEQDRAYLEGTCVEWLRRYLENGKDTLERADPPKTHVTHHPISDHE FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY FT TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK FT GGSYSQAACSDSAQGSDVSLTA" FT exon 477..746 FT /gene="HLA-B" FT /allele="B*08var" FT /number=2 FT exon 993..1268 FT /gene="HLA-B" FT /allele="B*08var" FT /number=3 FT exon 1841..2116 FT /gene="HLA-B" FT /allele="B*08var" FT /number=4 FT exon 2210..2326 FT /gene="HLA-B" FT /allele="B*08var" FT /number=5 FT exon 2768..2800 FT /gene="HLA-B" FT /allele="B*08var" FT /number=6 FT exon 2907..>2980 FT /gene="HLA-B" FT /allele="B*08var" FT /number=7 FT 3'UTR 2951..>2980 FT /gene="HLA-B" FT /allele="B*08var" XX SQ Sequence 2980 BP; 550 A; 898 C; 939 G; 593 T; 0 other; gaagtcccag gtcccggacg gggctctcag ggtctcaggc tccgagggcc gcgtctgcaa 60 tggggaggcg cagcgttggg gattccccac tcccctgagt ttcacttctt ctcccaactt 120 gtgtcgggtc cttcttccag gatactcgtg acgcatcccc acttcccact cccattgggt 180 gtcggatatc tagagaagcc aatcagcgtc gccggggtcc cagttctaaa gtccccacgc 240 acccacccgg actcagagtc tcctcagacg ccgagatgct ggtcatggcg ccccgaaccg 300 tcctcctgct gctctcggcg gccctggccc tgaccgagac ctgggccggt gagtgcgggt 360 cgggagggaa atggcctctg ccgggaggag cgaggggacc gcaggcgggg gcgcaggacc 420 tgaggagccg cgccgggagg agggtcgggc gggtctcagc ccctcctcgc ccccagcctc 480 ccactccatg aggtatttcg acaccgccat gtcccggccc ggccgcgggg agccccgctt 540 catctcagtg ggctacgtgg acgacacgca gttcgtgagg ttcgacagcg acgccgcgag 600 tccgagagag gagccgcggg cgccgtggat agagcaggag gggccggagt attgggaccg 660 gaacacacag atcttcaaga ccaacacaca gactgaccga gagagcctgc ggaacctgcg 720 cggctactac aaccagagcg aggccggtga gtgaccccgg cccggggcgc aggtcacgac 780 tccccatccc ccacggacgg cccgggtcgc cccgagtctc cgggtccgag atccgcctcc 840 ctgaggccgc gggacccgcc cagaccctcg accggcgaga gccccaggcg cgtttacccg 900 gtttcatttt cagttgaggc caaaatcccc gcgggttggt cggggcgggg cggggctcgg 960 ggggacgggg ctgaccgcgg ggccggggcc agggtctcac accctccaga gcatgtacgg 1020 ctgcgacgtg gggccggacg ggcgcctcct ccgcgggcat aaccagtacg cctacgacgg 1080 caaggattac atcgccctga acgaggacct gcgctcctgg accgcggcgg acaccgcggc 1140 tcagatcacc cagcgcaagt gggaggcggc ccgtgtggcg gagcaggaca gagcctacct 1200 ggagggcacg tgcgtggagt ggctccgcag atacctggag aacgggaagg acacgctgga 1260 gcgcgcgggt accaggggca gtggggagcc ttccccatct cctataggtc gccggggatg 1320 gcctcccacg agaagaggag gaaaatggga tcagcgctag aatgtcgccc tcccttgaat 1380 ggagaatggc atgagttttc ctgagtttcc tctgagggcc ccctcttctc tctagacaat 1440 taagggatga cgtctctgag gaaatggagg ggaagacagt ccctagaata ctgatcaggg 1500 gtcccctttg acccctgcag cagccttggg aaccgtgact tttcctctca ggccttgttc 1560 tctgcctcac actcagtgtg tttggggctc tgattccagc acttctgagt cactttacct 1620 ccactcagat caggagcaga agtccctgtt ccccgctcag agactcgaac tttccaatga 1680 ataggagatt atcccaggtg cctgcatccg ctggtgtctg ggttctgtgc cccttcccca 1740 ccccaggtgt cctgtccatt ctcaggctgg tcacatgggt ggtcctaggg tgtgccatga 1800 gagatgcaaa gcgcctgaat tttctgactc ttcccatcag accccccaaa gacacacgtg 1860 acccaccacc ccatctctga ccatgaggcc accctgaggt gctgggccct gggcttctac 1920 cctgcggaga tcacactgac ctggcagcgg gatggcgagg accaaactca ggacactgag 1980 cttgtggaga ccagaccagc aggagataga accttccaga agtgggcagc tgtggtggtg 2040 ccttctggag aagagcagag atacacatgc catgtacagc atgaggggct gccgaagccc 2100 ctcaccctga gatggggtaa ggagggggat gaggggtcat atctcttctc agggaaagca 2160 ggagcccttc agcagggtca gggcccctca tcttcccctc ctttcccaga gccgtcttcc 2220 cagtccaccg tccccatcgt gggcattgtt gctggcctgg ctgtcctagc agttgtggtc 2280 atcggagctg tggtcgctgc tgtgatgtgt aggaggaaga gctcaggtag ggaaggggtg 2340 aggggtgggg tctgggtttt cttgtcccac tgggggtttc aagccccagg tagaagtgtt 2400 ccctgcctca ttactgggat gcagcatcca cacaggggct aacgcagcct gggaccctgt 2460 gtgccagcac ttactctttt gtgcagcaca tgtgacaatg aaggacggat gtatcacctt 2520 ggtggttgtg gtgttggggt cctgattcca gcattcatga gtcaggggaa ggtccctgct 2580 aaggacagac cttaggaggg cagttggtcc aggacccaca cttgctttcc tcgtgtttcc 2640 tgatcctgcc ttgggtctgt agtcatactt ctggaaattc cttttgggtc caagacgagg 2700 aggttcctct aagatctcat ggccctgctt cctcccagtc ccctcacagg gcattttctt 2760 cccacaggtg gaaaaggagg gagctactct caggctgcgt gtaagtgatg ggggtgggag 2820 tgtggaggag ctcacccacc ccataattcc tcctgtccca cgtctcctgc gggctctgac 2880 caggtcctgt ttttgttcta ctccaggcag cgacagtgcc cagggctctg atgtgtctct 2940 cacagcttga aaaggtgaga ttcttggggt ctagagtggg 2980 //