Dbfetch
ID LT935653; SV 1; linear; genomic DNA; STD; HUM; 2951 BP. XX AC LT935653; XX PR Project:PRJEB22275; XX DT 28-JUN-2019 (Rel. 141, Created) DT 28-JUN-2019 (Rel. 141, Last updated, Version 1) XX DE Homo sapiens HLA-B gene for MHC class I antigen, allele "B*07:104ext" 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] RA Voorter E. C., Matern B.; RT ; RL Submitted (10-OCT-2017) to the INSDC. RL Maastricht University Medical Center, Transplantation Immunology, RL Transplantation Immunology, Tissue Typing, University Hospital Maastricht, RL P Debeylaan 25, 6202 AZ Maastricht, Netherlands XX DR MD5; 7f2779a972bec842714c617408b99587. XX FH Key Location/Qualifiers FH FT source 1..2951 FT /organism="Homo sapiens" FT /chromosome="6" FT /isolate="48062_SJ808/50" FT /mol_type="genomic DNA" FT /db_xref="taxon:9606" FT mRNA join(1..175,176..248,377..646,892..1167,1742..2017, FT 2111..2227,2669..2701,2808..2851,2852..2951) FT /gene="HLA-B" FT /allele="B*07:104ext" FT /product="MHC class I antigen" FT 5'UTR 1..175 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /note="5'UTR" FT CDS join(176..248,377..646,892..1167,1742..2017,2111..2227, FT 2669..2701,2808..2851) FT /pseudo FT /codon_start=1 FT /transl_table=1 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /note="MHC class I antigen" FT /db_xref="PSEUDO:SOH99631.1" FT exon 176..248 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=1 FT intron 249..376 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=1 FT exon 377..646 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=2 FT intron 647..891 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=2 FT exon 892..1167 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=3 FT intron 1168..1741 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=3 FT exon 1742..2017 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=4 FT intron 2018..2110 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=4 FT exon 2111..2227 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=5 FT intron 2228..2668 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=5 FT exon 2669..2701 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=6 FT intron 2702..2807 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=6 FT exon 2808..2851 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /number=7 FT 3'UTR 2852..2951 FT /gene="HLA-B" FT /allele="B*07:104ext" FT /note="3'UTR" XX SQ Sequence 2951 BP; 546 A; 866 C; 941 G; 598 T; 0 other; ttcacttctt ctcccaactt gtgtcgggtc cttcttccag gatactcgtg acgcgtcccc 60 acttcccact cccattgggt attggatatc tagagaagcc aatcagcgtc gccgcggtcc 120 cagttctaaa gtccccacgc acccacccgg actcagagtc tcctcagacg ccgagatgct 180 ggtcatggcg ccccgaaccg tcctcctgct gctctcggcg gccctggccc tgaccgagac 240 ctgggccggt gagtgcgggt cgggagggaa atggcctctg ccgggaggag cgaggggacc 300 gcaggcgggg gcgcaggacc tgaggagccg cgccgggagg agggtcgggc gggtctcagc 360 ccctcctcac ccccaggctc ccactccatg aggtatttct acacctccgt gtcccggccc 420 ggccgcgggg agccccgctt catctcagtg ggctacgtgg acgacaccca gttcgtgagg 480 ttcgacagcg gcgccgcgag tccgagagag gagccgcggg cgccgtggat agagcaggag 540 gggccggagt attgggaccg gaacacacag atctacaagg cccaggcaca gactgaccga 600 gagagcctgc ggaacctgcg cggctactac aaccagagcg aggccggtga gtgaccccgg 660 cccggggcgc aggtcacgac tccccatccc ccacgtacgg cccgggtcgc cccgagtctc 720 cgggtccgag atccgcctcc ctgaggccgc gggacccgcc cagaccctcg accggcgaga 780 gccccaggcg cgtttacccg gtttcatttt cagttgaggc caaaatcccc gcgggttggt 840 cggggcgggg cggggctcgg gggactgggc tgaccgcggg gccggggcca gggtctcaca 900 ccctccagag catgtacggc tgcgacgtgg ggccggacgg gcgcctcctc cgcgggcatg 960 accagtacgc ctacgacggc aaggattaca tcgccctgaa cgaggacctg cgctcctgga 1020 ccgccgcgga cacggcggct cagatcaccc agcgcaagtg ggaggcggcc cgtgaggcgg 1080 agcagcggag agcctacctg gagggcgagt gcgtggagtg gctccgcaga tacctggaga 1140 acgggaagga caagctggag cgcgctggta ccaggggcag tggggagcct tccccatctc 1200 ctataggtcg ccggggatgg cctcccacga gaagaggagg aaaatgggat cagcgctaga 1260 atgtcgccct ccgttgaatg gagaatggca tgagttttcc tgagtttcct ctgagggccc 1320 cctcttctct ctagacaatt aaggaatgac gtctctgagg aaatggaggg gaagacagtc 1380 cctagaatac tgatcagggg tcccctttga cccctgcagc agccttggga accgtgactt 1440 ttcctctcag gccttgttct ctgcctcaca ctcagtgtgt ttggggctct gattccagca 1500 cttctgagtc actttacctc cactcagatc aggagcagaa gtccctgttc cccgctcaga 1560 gactcgaact ttccaatgaa taggagatta tcccaggtgc ctgcgtccag gctggtgtct 1620 gggttctgtg ccccttcccc accccaggtg tcctgtccat tctcaggctg gtcacatggg 1680 tggtcctagg gtgtcccatg aaagatgcaa agcgcctgaa ttttctgact cttcccatca 1740 gaccccccaa agacacacgt gacccaccac cccatctctg accatgaggc caccctgagg 1800 tgctgggccc tgggtttcta ccctgcggag atcacactga cctggcagcg ggatggcgag 1860 gaccaaactc aggacactga gcttgtggag accagaccag caggagatag aaccttccag 1920 aagtgggcag ctgtggtggt gccttctgga gaagagcaga gatacacatg ccatgtacag 1980 catgaggggc tgccgaagcc cctcaccctg agatggggta aggaggggga tgaggggtca 2040 tatctcttct cagggaaagc aggagccctt cagcagggtc agggcccctc atcttcccct 2100 cctttcccag agccgtcttc ccagtccacc gtccccatcg tgggcattgt tgctggcctg 2160 gctgtcctag cagttgtggt catcggagct gtggtcgctg ctgtgatgtg taggaggaag 2220 agttcaggta gggaaggggt gaggggtggg gtctgggttt tcttgtccca ctgggggttt 2280 caagccccag gtagaagtgt tccctgcctc attactggga agcagcatgc acacaggggc 2340 taacgcagcc tgggaccctg tgtgccagca cttactcttt tgtgcagcac atgtgacaat 2400 gaaggatgga tgtatcacct tgatggttgt ggtgttgggg tcctgattcc agcattcatg 2460 agtcagggga aggtccctgc taaggacaga ccttaggagg gcagttggtc caggacccac 2520 acttgctttc ctcgtgtttc ctgatcctgc cctgggtctg tagtcatact tctggaaatt 2580 ccttttgggt ccaagactag gaggttcctc taagatctca tggccctgct tcctcccagt 2640 gccctcacag gacattttct tcccacaggt ggaaaaggag ggagctactc tcaggctgcg 2700 tgtaagtggt gggggtggga gtgtggagga gctcacccac cccataattc ctcctgtccc 2760 acgtctcctg cgggctctga ccaggtcctg tttttgttct actccaggca gcgacagtgc 2820 ccagggctct gatgtgtctc tcacagcttg aaaaggtgag attcttgggg tctagagtgg 2880 gtggggtggc gggtctgggg gtgggtgggg cagaggggaa aggcctgggt aatggggatt 2940 ctttgattgg g 2951 //