Canonical Allele Identifier: CA136836028
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs879151417

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356407_31356432delinsGGTCGCAGCCATACATCGTCTGCCAA , CM000668.2:g.31356407_31356432delinsGGTCGCAGCCATACATCGTCTGCCAA GRCh38
NC_000006.11:g.31324184_31324209delinsGGTCGCAGCCATACATCGTCTGCCAA , CM000668.1:g.31324184_31324209delinsGGTCGCAGCCATACATCGTCTGCCAA GRCh37
NC_000006.10:g.31432163_31432188delinsGGTCGCAGCCATACATCGTCTGCCAA NCBI36
NG_023187.1:g.5781_5806delinsTTGGCAGACGATGTATGGCTGCGACC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1827_1852delinsTTGGCAGACGATGTATGGCTGCGACC
ENST00000481849.6:n.1827_1852delinsTTGGCAGACGATGTATGGCTGCGACC
ENST00000497377.6:n.1827_1852delinsTTGGCAGACGATGTATGGCTGCGACC
ENST00000640094.2:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000491275.2:p.Leu119_Val127delinsTr...
ENST00000696558.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000512716.1:p.Leu119_Val127delinsTr...
ENST00000696559.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000512717.1:p.Leu119_Val127delinsTr...
ENST00000696560.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000512718.1:p.Leu119_Val127delinsTr...
ENST00000696561.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000512719.1:p.Leu119_Val127delinsTr...
ENST00000696562.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000512720.1:p.Leu119_Val127delinsTr...
ENST00000412585.7:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC MANE Select ENSP00000399168.2:p.Leu119_Val127delinsTr...
ENST00000412585.6:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000399168.2:p.Leu119_Val127delinsTr...
ENST00000434333.1:c.387_412delinsTTGGCAGACGATGTATGGCTGCGACC ENSP00000405931.1:p.Leu130_Val138delinsTr...
ENST00000474381.1:n.229_254delinsTTGGCAGACGATGTATGGCTGCGACC
ENST00000498007.1:n.620_645delinsTTGGCAGACGATGTATGGCTGCGACC
NM_005514.6:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC NP_005505.2:p.Leu119_Val127delinsTrpGlnTh...
XM_011514556.1:c.387_412delinsTTGGCAGACGATGTATGGCTGCGACC XP_011512858.1:p.Leu130_Val138delinsTrpGl...
XM_011514557.1:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC XP_011512859.1:p.Leu119_Val127delinsTrpGl...
XR_926175.1:n.364_389delinsTTGGCAGACGATGTATGGCTGCGACC
NM_005514.7:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC NP_005505.2:p.Leu119_Val127delinsTrpGlnTh...
NM_005514.8:c.354_379delinsTTGGCAGACGATGTATGGCTGCGACC MANE Select NP_005505.2:p.Leu119_Val127delinsTrpGlnTh...