Dbfetch
ID MN003040; SV 1; linear; genomic DNA; STD; HUM; 2726 BP. XX AC MN003040; 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_06376 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 XX RN [1] RP 1-2726 RA Cereb N., Yang S.Y.; RT "HLA new alleles found by Histogenetics"; RL Unpublished. XX RN [2] RP 1-2726 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; 75925e6e5c798cf79278f19990b254c6. XX FH Key Location/Qualifiers FH FT source 1..2726 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /clone="B_112399_06376" FT /db_xref="taxon:9606" FT gene 1..>2726 FT /gene="HLA-B" FT mRNA join(1..109,239..508,755..1030,1606..1881,1986..2102, FT 2544..2576,2683..>2726) 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..109,239..508,755..1030,1606..1881,1986..2102, FT 2544..2576,2683..2726) FT /codon_start=1 FT /gene="HLA-B" FT /product="MHC class I antigen" FT /protein_id="QDK62569.1" FT /translation="MRVTAPRTVLLLLWGAVALTETWAGSHSMRYFYTAMSRPGRGEPR FT FIAVGYVDDTQFVRFDSDAASPRTEPRAPWIEQEGPEYWDGETRNMKASAQTYRENLRI FT ALRYYNQSEAGSHIIQRMYGCDLGPDGRLLRGHDQSAYDGKDYIALNEDLSSWTAADTA FT AQITQRKWEAARVAEQLRAYLEGLCVEWLRRYLENGKETLQRADPPKTHVTHHPVSDHE FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY FT TCHVQHEGLPKPLTLRWEPSSQSTIPIVGIVAGLAVLAVVVIGAVVATVMCRRKSSGGK FT GGSYSQAASSDSAQGSDVSLTA" FT intron 110..238 FT /gene="HLA-B" FT /number=1 FT exon 239..508 FT /gene="HLA-B" FT /number=2 FT intron 509..754 FT /gene="HLA-B" FT /number=2 FT exon 755..1030 FT /gene="HLA-B" FT /number=3 FT intron 1031..1605 FT /gene="HLA-B" FT /number=3 FT exon 1606..1881 FT /gene="HLA-B" FT /number=4 FT intron 1882..1985 FT /gene="HLA-B" FT /number=4 FT exon 1986..2102 FT /gene="HLA-B" FT /number=5 FT intron 2103..2543 FT /gene="HLA-B" FT /number=5 FT exon 2544..2576 FT /gene="HLA-B" FT /number=6 FT intron 2577..2682 FT /gene="HLA-B" FT /number=6 FT exon 2683..>2726 FT /gene="HLA-B" FT /number=7 XX SQ Sequence 2726 BP; 504 A; 815 C; 868 G; 539 T; 0 other; cacccacccg gactcagaat ctcctcagac gccgagatgc gggtcacggc gccccgaacc 60 gtcctcctgc tgctctgggg ggcagtggcc ctgaccgaga cctgggccgg tgagtgcggg 120 gtcgggaggg aaatggcctc tgtggggagg agcgagggga ccgcaggcgg gggcgcagga 180 cctgaggagc cgcgccggga ggagggtcgg gcgggtctca gcccctcctc gcccccaggc 240 tcccactcca tgaggtattt ctacaccgcc atgtcccggc ccggccgcgg ggagccccgc 300 ttcatcgcag tgggctacgt ggacgacacc cagttcgtga ggttcgacag cgacgccgcg 360 agtccgagga cggagccccg ggcgccatgg atagagcagg aggggccgga gtattgggac 420 ggggagacac ggaacatgaa ggcctccgcg cagacttacc gagagaacct gcggatcgcg 480 ctccgctact acaaccagag cgaggccggt gagtgacccc ggcccggggc gcaggtcacg 540 actccccatc ccccacgtac ggcccgggtc gccccgagtc tccgggtccg agatccgcct 600 ccctgaggcc gcgggacccg cccagaccct cgaccggcga gagccccagg cgcgtttacc 660 cggtttcatt ttcagttgag gccaaaatcc ccgcgggttg gtcggggcgg ggcggggctc 720 gggggacggg gctgacccgc ggggccgggg ccagggtctc acatcatcca gaggatgtat 780 ggctgcgacc tggggcccga cgggcgcctc ctccgcgggc atgaccagtc cgcctacgac 840 ggcaaggatt acatcgccct gaacgaggac ctgagctcct ggaccgcggc ggacaccgcg 900 gctcagatca cccagcgcaa gtgggaggcg gcccgtgtgg cggagcagct gagagcctac 960 ctggagggcc tgtgcgtgga gtggctccgc agatacctgg agaacgggaa ggagacgctg 1020 cagcgcgcgg gtaccagggg cagtggggag ccttccccat ctcctatagg tcgccgggga 1080 tggcctccca cgagaagagg aggaaaatgg gatcagcgct agaatgtcgc cctcccttga 1140 atggagaatg gcatgagttt tcctgagttt cctctgaggg ccccctcttc tctctaggac 1200 aattaaggga tgacgtctct gaggaaatgg aggggaagac agtccctaga atactgatca 1260 ggggtcccct ttgacccctg cagcagcctt gggaaccgtg acttttcctc tcaggccttg 1320 ttctctgcct cacactcagt gtgtttgggg ctctgattcc agcacttctg agtcacttta 1380 cctccactca gatcaggagc agaagtccct gttccccgct cagagactcg aactttccaa 1440 tgaataggag attatcccag gtgcctgcgt ccaggctggt gtctgggttc tgtgcccctt 1500 ccccacacca ggtgtcctgt ccattctcag gctggtcaca tgggtggtcc tagggtgtcc 1560 catgagagat gcaaagcgcc tgaattttct gactcttccc atcagacccc ccaaagacac 1620 acgtgaccca ccaccccgtc tctgaccatg aggccaccct gaggtgctgg gccctgggct 1680 tctaccctgc ggagatcaca ctgacctggc agcgggatgg cgaggaccaa actcaggaca 1740 ctgagcttgt ggagaccaga ccagcaggag atagaacctt ccagaagtgg gcagctgtgg 1800 tggtgccttc tggagaagag cagagataca catgccatgt acagcatgag gggctgccga 1860 agcccctcac cctgagatgg ggtaaggagg gggatgaggg gtcatatctc ttctcaggga 1920 aagcaggagc ccttctggag cccttcagca gggtcagggc ccctcgtctt cccctccttt 1980 cccagagcca tcttcccagt ccaccatccc catcgtgggc attgttgctg gcctggctgt 2040 cctagcagtt gtggtcatcg gagctgtggt cgctactgtg atgtgtagga ggaagagctc 2100 aggtagggaa ggggtgaggg gtggggtctg ggttttcttg tcccactggg ggtttcaagc 2160 cccaggtaga agtgttccct gcctcattac tgggaagcag catccacaca ggggctaacg 2220 cagcctggga ccctgtgtgc cagcacttac tcttttgtgc agcacatgtg acaatgaagg 2280 acggatgtat caccttgatg gttgtggtgt tggggtcctg atttcagcat tcatgagtca 2340 ggggaaggtc cctgctaagg acagacctta ggagggcagt tggtccagga cccacacttg 2400 ctttcctcgt gtttcctgat cctgccttgg gtctgtagtc atacttctgg aaattccttt 2460 tgggtccaag acgaggaggt tcctctaaga tctcatggcc ctgcttcctc ccagtcccct 2520 cacaggacat tttcttccca caggtggaaa aggagggagc tactctcagg ctgcgtgtaa 2580 gtggtggggg tgggagtgtg gaggagctca cccaccccat aattcctcct gtcccacgtc 2640 tcctgcgggc tctgaccagg tcctgttttt gttctactcc agccagcgac agtgcccagg 2700 gctctgatgt gtctctcaca gcttga 2726 //