Dbfetch
ID MK058661; SV 1; linear; genomic DNA; STD; HUM; 2723 BP. XX AC MK058661; XX DT 03-OCT-2019 (Rel. 142, Created) DT 03-OCT-2019 (Rel. 142, Last updated, Version 1) XX DE Homo sapiens clone B_112135_05672 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 XX RN [1] RP 1-2723 RA Cereb N., Yang S.Y.; RT "HLA new alleles found by Histogenetics"; RL Unpublished. XX RN [2] RP 1-2723 RA Cereb N., Yang S.Y.; RT ; RL Submitted (15-OCT-2018) to the INSDC. RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA XX DR MD5; 1b3ae2dd777bc4afe4f0aa0fd8e08044. XX FH Key Location/Qualifiers FH FT source 1..2723 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /clone="B_112135_05672" FT /db_xref="taxon:9606" FT gene 1..>2723 FT /gene="HLA-B" FT mRNA join(1..109,239..508,755..1030,1603..1878,1983..2099, FT 2541..2573,2680..>2723) 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..1030,1603..1878,1983..2099, FT 2541..2573,2680..2723) FT /codon_start=1 FT /gene="HLA-B" FT /product="MHC class I antigen" FT /protein_id="AZL48726.1" FT /translation="MRVTAPRTLLLLLWGAVALTETWAGSHSMRYFHTSVSRPGRGEPR FT FISVGYVDDTQFVRFDSDAASPRTEPRAPWIEQEGPEYWDRETQISKTNTQTYREDLRT FT LLRYYNQSEAGSHTIQRMSGCDVGPDGRLLRGYNQFAYDGKDYIALNEDLRSWTAADTA FT AQITQRKWEAARVAEQDRAYLEGTCVEWLRRYLENGKETLQRADPPKTHVTHHPISDHE 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..1602 FT /gene="HLA-B" FT /number=3 FT exon 1603..1878 FT /gene="HLA-B" FT /number=4 FT intron 1879..1982 FT /gene="HLA-B" FT /number=4 FT exon 1983..2099 FT /gene="HLA-B" FT /number=5 FT intron 2100..2540 FT /gene="HLA-B" FT /number=5 FT exon 2541..2573 FT /gene="HLA-B" FT /number=6 FT intron 2574..2679 FT /gene="HLA-B" FT /number=6 FT exon 2680..>2723 FT /gene="HLA-B" FT /number=7 XX SQ Sequence 2723 BP; 507 A; 821 C; 856 G; 539 T; 0 other; cacccacccg gactcagaat ctcctcagac gccgagatgc gggtcacggc gccccgaacc 60 ctcctcctgc tgctctgggg ggcagtggcc ctgaccgaga cctgggctgg tgagtgcggg 120 gtcggcaggg aaatggcctc tgtggggagg agcgagggga ccgcaggcgg gggcgcagga 180 cccggggagc cgcgccggga ggagggtcgg gcgggtctca gcccctcctc gcccccaggc 240 tcccactcca tgaggtattt ccacacctcc gtgtcccggc ccggccgcgg ggagccccgc 300 ttcatctcag tgggctacgt ggacgacacc cagttcgtga ggttcgacag cgacgccgcg 360 agtccgagga cggagccccg ggcgccgtgg atagagcagg aggggccgga gtattgggac 420 cgggagacac agatctccaa gaccaacaca cagacttacc gagaggacct gcggaccctg 480 ctccgctact acaaccagag cgaggccggt gagtgacccc ggcccggggc gcaggtcacg 540 actccccatc ccccacgtac ggcccgggtc gccccgagtc tccgggtccg agatccgccc 600 ccctgaggcc gcgggacccg cccagaccct cgaccggcga gagccccagg cgcgtttacc 660 cggtttcatt ttcagttgag gccaaaatcc ccgcgggttg gtcggggcgg ggcggggctc 720 ggggggacgg ggctgaccgc ggggccgggg ccagggtctc acaccatcca gaggatgtct 780 ggctgcgacg tggggccgga cgggcgcctc ctccgcgggt ataaccagtt cgcctacgac 840 ggcaaggatt acatcgccct gaacgaggac ctgcgctcct ggaccgcggc ggacaccgcg 900 gctcagatca cccagcgcaa gtgggaggcg gcccgtgtgg cggagcagga cagagcctac 960 ctggagggca cgtgcgtgga 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 gggaaccatg acttttcctc tcaggccttg 1320 ttctctgcct cacactcagt gtgtttgggg ctctgattcc agcacttctg agtcacttta 1380 cctccactca gatcaggagc agaagtctct gttccccgct cagagactcg aactttccaa 1440 tgaatagatt atcccaggtg cctgcgtcca ggctggtgtc tgggttctgt gccccttccc 1500 caccccaggt gtcctgtcca ttctcaggct ggtcacatgg gtggtcctag ggtgtcccat 1560 gagagatgca aagcgcctga attttctgac tcttcccatc agacccccca aagacacatg 1620 tgacccacca ccccatctct gaccatgagg ccaccctgag gtgctgggcc ctgggcttct 1680 accctgcgga gatcacactg acctggcagc gggatggcga ggaccaaact caggacaccg 1740 agcttgtgga gaccagacca gcaggagata gaaccttcca gaagtgggca gctgtggtgg 1800 tgccttctgg agaagagcag agatacacat gccatgtaca gcatgagggg ctgccgaagc 1860 ccctcaccct gagatggggt aaggaggggg atgaggggtc atatctcttc tcagggaaag 1920 caggagccct tctggagccc ttcagcaggg tcaggacccc tcatcttccc ctcctttccc 1980 agagccatct tcccagtcca ccatccccat cgtgggcatt gttgctggcc tggctgtcct 2040 agcagttgtg gtcatcggag ctgtggtcgc tactgtgatg tgtaggagga agagctcagg 2100 tagggaaggg gtgaggggtg gggtctgggt tttcttgtcc cactgggggt ttcaagcccc 2160 aggtagaagt gttccctgcc tcattactgg gaagcagcat ccacacaggg gctaacgcag 2220 cctgggaccc tgtgtgccag cacttactct tttgtgcagc acatgtgaca atgaaggacg 2280 gatgtatcac cttgatggtt gtggtgttgg ggtcctgatt ccagcattca tgagtcaggg 2340 gaaggtccct gctaaggaca gaccttagga gggcagttgg tccaggaccc acacttgctt 2400 tcctcgtgtt tcctgatcct gccttgggtc tgtagtcata cttctggaaa ttccttttgg 2460 ttccaagacg aggaggttcc tctaagatct catggccctg cttcctccca gtcccctcac 2520 aggacatttt cttcccacag gtggaaaagg agggagctac tctcaggctg cgtgtaagtg 2580 gtgggggtgg gagtgtggag gagctcaccc accccataat tcctcctgtc ccacgtctcc 2640 tgcgggctct gaccaggtcc tgtttttgtt ctactccagc cagcgacagt gcccagggct 2700 ctgatgtgtc tctcacagct tga 2723 //