Dbfetch

ID   HM140623; SV 1; linear; genomic DNA; STD; HUM; 2057 BP.
XX
AC   HM140623;
XX
DT   27-AUG-2010 (Rel. 105, Created)
DT   27-AUG-2010 (Rel. 105, Last updated, Version 1)
XX
DE   Homo sapiens MHC class I antigen-like (HLA-B) gene, HLA-B*40 variant
DE   allele, partial sequence.
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   1-2057
RA   Park N.-R., Jun J.-H., Oh H.-B., Kwon O.-J.;
RT   "5 bp inserted HLA-B*40 New allele";
RL   Unpublished.
XX
RN   [2]
RP   1-2057
RA   Park N.-R., Jun J.-H., Oh H.-B., Kwon O.-J.;
RT   ;
RL   Submitted (20-APR-2010) to the INSDC.
RL   Molecular Genetics, Biowithus, #508, Woolim e-BIZ Center, 280-21,
RL   Seongsu-dong 2-ga, Seongdong-gu, Seoul 133-120, Republic of Korea
XX
DR   MD5; 0178a30e65e556f5df4d5c21fab0dc57.
DR   IMGT/HLA; B*40:155:01N; HLA05842.
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..2057
FT                   /organism="Homo sapiens"
FT                   /chromosome="6"
FT                   /map="6p21"
FT                   /mol_type="genomic DNA"
FT                   /db_xref="taxon:9606"
FT   gene            <1..>2057
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT   misc_feature    join(<1..73,202..471,717..997,1572..1847,1941..>2057)
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /note="similar to MHC class I antigen; translation contains
FT                   6 stop codons"
FT   exon            <1..73
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /number=1
FT   exon            202..471
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /number=2
FT   exon            717..997
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /number=3
FT   exon            1572..1847
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /number=4
FT   exon            1941..>2057
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*40 variant"
FT                   /number=5
XX
SQ   Sequence 2057 BP; 389 A; 633 C; 667 G; 368 T; 0 other;
     atgcgggtca cggcaccccg aaccgtcctc ctgctgctct cggcggccct ggccctgacc        60
     gagacctggg cgggtgagtg cgggtcggca gggaaatggc ctctgtgggg aggagcgagg       120
     ggaccgcagg cgggggcgca ggacccgggg agccgcgccg ggaggagggt cgggcgggtc       180
     tcagctcctc ctcgccccca ggctcccact ccatgaggta tttccacacc gccatgtccc       240
     ggcccggccg cggggagccc cgcttcatca ccgtgggcta cgtggacgac acgctgttcg       300
     tgaggttcga cagcgacgcc acgagtccga ggaaggagcc gcgggcgcca tggatagagc       360
     aggaggggcc ggagtattgg gaccgggaga cacagatctc caagaccaac acacagactt       420
     accgagagag cctgcggaac ctgcgcggct actacaacca gagcgaggcc ggtgagtgac       480
     cccggcccgg ggcgcaggtc acgactcccc atcccccacg tacggcccgg gtcgccccga       540
     gtctccgggt ccgagatccg accccctgag gccgcgggac ccgcccagac cctcgaccgg       600
     cgagagcccc aggcgcgttt acccggtttc attttcagtt gaggccaaaa tccccgcggg       660
     ttggtcgggg cggggcgggg ctcgggggac tgggctgacc gcggggccgg ggccagggtc       720
     tcacaccctc cagaggatgt acggctgcga cgtggggccg gacgggcgcc tcctccgcgg       780
     gcataaccag tacgcctacg acggcaagga ttacatcgcc ctgaacgagg acctgcgctc       840
     ctggaccgcc gcggacacgg cggctcagat ctcccagcgc aagttggagg cggcccgtgt       900
     ggcggagcag ctgagagcct acctggaggg cgagtgcgtg gagtggctcc gcagatacct       960
     ggagaacaga acgggaagga caagctggag cgcgctggta ccaggggcag tggggagcct      1020
     tccccatctc ctataggtcg ccggggatgg cctcccacga gaagaggagg aaaatgggat      1080
     cagcgctaga atgtcgccct ccgttgaatg gagaatggca tgagttttcc tgagtttcct      1140
     ctgagggccc cctcttctct ctagacaatt aaggaatgac gtctctgagg aaatggaggg      1200
     gaagacagtc cctagaatac tgatcagggg tcccctttga cccctgcagc agccttggga      1260
     accgtgactt ttcctctcag gccttgttct ctgcctcaca ctcagtgtgt ttggggctct      1320
     gattccagca cttctgagtc actttacctc cactcagatc aggagcagaa gtccctgttc      1380
     cccgctcaga gactcgaact ttccaatgaa taggagatta tcccaggtgc ctgcgtccag      1440
     gctggtgtct gggttctgtg ccccttcccc accccaggtg tcctgtccat tctcaggctg      1500
     gtcacatggg tggtcctagg gtgtcccatg aaagatgcaa agcgcctgaa ttttctgact      1560
     cttcccatca gaccccccaa agacacacgt gacccaccac cccatctctg accatgaggc      1620
     caccctgagg tgctgggccc tgggtttcta ccctgcggag atcacactga cctggcagcg      1680
     ggatggcgag gaccaaactc aggacactga gcttgtggag accagaccag caggagatag      1740
     aaccttccag aagtgggcag ctgtggtggt gccttctgga gaagagcaga gatacacatg      1800
     ccatgtacag catgaggggc tgccgaagcc cctcaccctg agatggggta aggaggggga      1860
     tgaggggtca tatctcttct cagggaaagc aggagccctt cagcagggtc agggcccctc      1920
     atcttcccct cctttcccag agccgtcttc ccagtccacc gtccccatcg tgggcattgt      1980
     tgctggcctg gctgtcctag cagttgtggt catcggagct gtggtcgctg ctgtgatgtg      2040
     taggaggaag agttcag                                                     2057
//