Dbfetch
ID MH173363; SV 1; linear; genomic DNA; STD; HUM; 2712 BP. XX AC MH173363; XX DT 24-MAY-2019 (Rel. 140, Created) DT 24-MAY-2019 (Rel. 140, Last updated, Version 1) XX DE Homo sapiens clone B_111912_05012 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 XX RN [1] RP 1-2712 RA Cereb N., Yang S.Y.; RT "HLA new alleles found by Histogenetics"; RL Unpublished. XX RN [2] RP 1-2712 RA Cereb N., Yang S.Y.; RT ; RL Submitted (19-MAR-2018) to the INSDC. RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA XX DR MD5; d646aebc87d18d49e64cdb2a2ff437e2. XX FH Key Location/Qualifiers FH FT source 1..2712 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /clone="B_111912_05012" FT /db_xref="taxon:9606" FT gene <1..>2712 FT /gene="HLA-B" FT mRNA join(<1..109,238..507,752..1027,1603..1878,1972..2088, FT 2530..2562,2669..>2712) 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..507,752..1027,1603..1878,1972..2088, FT 2530..2562,2669..2712) FT /codon_start=1 FT /gene="HLA-B" FT /product="MHC class I antigen" FT /db_xref="GOA:A0A4P2SR34" FT /db_xref="UniProtKB/TrEMBL:A0A4P2SR34" FT /protein_id="AWM62415.1" FT /translation="MRVTAPRTLLLLLWGALALTETWAGSHSMRYFHTSVSRPGRGEPR FT FITVGYVDDTLFVRFDSDAASPREEPRAPWIEQEGPEYWDRETQICKAKAQTDREDLRT FT LLRYYNQSEAGSHTLQNMYGCDVGPDGRLLRGYHQDAYDGKDYIALNEDLSSWTAADTA FT AQITQRKWEAARVAEQLRAYLEGECVEWLRRYLENGKETLQRADPPKTHVTHHPISDHE FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY FT TCHVQHEGLPKPLTLRWEPSSQSTVPIVGIVAGLAVLAVVVIGAVVAAVMCRRKSSGGK FT GGSYSQAACSDSAQGSDVSLTA" 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..751 FT /gene="HLA-B" FT /number=2 FT exon 752..1027 FT /gene="HLA-B" FT /number=3 FT intron 1028..1602 FT /gene="HLA-B" FT /number=3 FT exon 1603..1878 FT /gene="HLA-B" FT /number=4 FT intron 1879..1971 FT /gene="HLA-B" FT /number=4 FT exon 1972..2088 FT /gene="HLA-B" FT /number=5 FT intron 2089..2529 FT /gene="HLA-B" FT /number=5 FT exon 2530..2562 FT /gene="HLA-B" FT /number=6 FT intron 2563..2668 FT /gene="HLA-B" FT /number=6 FT exon 2669..>2712 FT /gene="HLA-B" FT /number=7 XX SQ Sequence 2712 BP; 499 A; 814 C; 868 G; 531 T; 0 other; cacccacccg gactcagaat ctcctcagac gccgagatgc gggtcacggc gccccgaacc 60 ctcctcctgc tgctctgggg ggccctggcc ctgaccgaga cctgggccgg tgagtgcggg 120 tcggcaggga aatggcctct gtggggagga gcgaggggac cgcaggcggg ggcgcaggac 180 ccggggagcc gcgccgggag gagggtcggg cgggtctcag cccctcctcg cccccaggct 240 cccactccat gaggtatttc cacacctccg tgtcccggcc cggccgcggg gagccccgct 300 tcatcaccgt gggctacgtg gacgacacgc tgttcgtgag gttcgacagc gacgccgcga 360 gtccgagaga ggagccgcgg gcgccgtgga tagagcagga ggggccggag tattgggacc 420 gggagacaca gatctgcaag gccaaggcac agactgaccg agaggacctg cggaccctgc 480 tccgctacta caaccagagc gaggccggtg agtgaccccg gcccggggcg caggtcacga 540 ctccccatcc cccacgtacg gcccgggtcg ccccgagtct ccgggtccga gatccgcccc 600 cgaggccgcg ggacccgccc agaccctcga ccggcgagag ccccaggcgc gtttacccgg 660 tttcattttc agttgaggcc aaaatccccg cgggttggtc ggggcggggc ggggctcggg 720 gggacggggc tgaccgcggg ggcggggcca gggtctcaca ccctccagaa tatgtatggc 780 tgcgacgtgg ggccggacgg gcgcctcctc cgcgggtacc accaggacgc ctacgacggc 840 aaggattaca tcgccctgaa cgaggacctg agctcctgga ccgccgcgga cacggcggct 900 cagatcaccc agcgcaagtg ggaggcggcc cgtgtggcgg agcagctgag agcctacctg 960 gagggcgagt gcgtggagtg gctccgcaga tacctggaga acgggaagga gacgctgcag 1020 cgcgcgggta ccaggggcag tggggagcct tccccatctc ctataggtcg ccggggatgg 1080 cctcccacga gaagaggagg aaaatgggat cagcgctaga atgtcgccct cccttgaatg 1140 gagaatggca tgagttttcc tgagtttcct ctgagggccc cctcttctct ctaggacaat 1200 taagggatga cgtctctgag gaaatggagg ggaagacagt ccctagaata ctgatcaggg 1260 gtcccctttg acccctgcag cagccttggg aaccgtgact tttcctctca ggccttgttc 1320 tctgcctcac actcagtgtg tttggggctc tgattccagc acttctgagt cactttacct 1380 ccactcagat caggagcaga agtccctgtt ccccgctcag agactcgaac tttccaatga 1440 ataggagatt atcccaggtg cctgcgtcca ggctggtgtc tgggttctgt gccccttccc 1500 caccccaggt gtcctgtcca ttctcaggct ggtcacatgg gtggtcctag ggtgtcccat 1560 gagagatgca aagcgcctga attttctgac tcttcccatc agacccccca aagacacacg 1620 tgacccacca ccccatctct gaccatgagg ccaccctgag gtgctgggcc ctgggcttct 1680 accctgcgga gatcacactg acctggcagc gggatggcga ggaccaaact caggacactg 1740 agcttgtgga gaccagacca gcaggagata gaaccttcca gaagtgggca gctgtggtgg 1800 tgccttctgg agaagagcag agatacacat gccatgtaca gcatgagggg ctgccgaagc 1860 ccctcaccct gagatggggt aaggaggggg atgaggggtc atatctcttc tcagggaaag 1920 caggagccct tcagcagggt cagggcccct catcttccct tcctttccca gagccgtctt 1980 cccagtccac cgtccccatc gtgggcattg ttgctggcct ggctgtccta gcagttgtgg 2040 tcatcggagc tgtggtcgct gctgtgatgt gtaggaggaa gagctcaggt agggaagggg 2100 tgaggggtgg ggtctgagtt ttcttgtccc actgggggtt tcaagcccca ggtagaagtg 2160 ttccctgcct cattactggg aagcagcatc cacacagggg ctaacgcagc ctgggaccct 2220 gtgtgccagc acttactctt ttgtgcagca catgtgacaa tgaaggacgg atgtatcacc 2280 ttggtggttg tggtgttggg gtcctgattc cagcattcat gagtcagggg aaggtccctg 2340 ctaaggacag accttaggag ggcagttggt ccaggaccca cacttgcttt cctcgtgttt 2400 cctgatcctg ccttgggtct gtagtcatac ttctggaaat tccttttggg tccaagacga 2460 ggaggttcct ctaagatctc atggccctgc ttcctcccag tcccctcaca gggcattttc 2520 ttcccacagg tggaaaagga gggagctact ctcaggctgc gtgtaagtga tgggggtggg 2580 agtgtggagg agctcaccca ccccctaatt cctcctgtcc cacgtctcct gcgggctctg 2640 accaggtcct gtttttgttc tactccaggc agcgacagtg cccagggctc tgatgtgtct 2700 ctcacagctt ga 2712 //