Canonical Allele Identifier: CA917712301
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs758686214

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356422_31356423insCGTCTGCCAA , CM000668.2:g.31356422_31356423insCGTCTGCCAA GRCh38
NC_000006.11:g.31324199_31324200insCGTCTGCCAA , CM000668.1:g.31324199_31324200insCGTCTGCCAA GRCh37
NC_000006.10:g.31432178_31432179insCGTCTGCCAA NCBI36
NG_023187.1:g.5790_5791insTTGGCAGACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1836_1837insTTGGCAGACG
ENST00000481849.6:n.1836_1837insTTGGCAGACG
ENST00000497377.6:n.1836_1837insTTGGCAGACG
ENST00000640094.2:c.363_364insTTGGCAGACG ENSP00000491275.2:p.Met122LeufsTer20
ENST00000696558.1:c.363_364insTTGGCAGACG ENSP00000512716.1:p.Met122LeufsTer20
ENST00000696559.1:c.363_364insTTGGCAGACG ENSP00000512717.1:p.Met122LeufsTer20
ENST00000696560.1:c.363_364insTTGGCAGACG ENSP00000512718.1:p.Met122LeufsTer20
ENST00000696561.1:c.363_364insTTGGCAGACG ENSP00000512719.1:p.Met122LeufsTer20
ENST00000696562.1:c.363_364insTTGGCAGACG ENSP00000512720.1:p.Met122LeufsTer20
ENST00000412585.7:c.363_364insTTGGCAGACG MANE Select ENSP00000399168.2:p.Met122LeufsTer20
ENST00000412585.6:c.363_364insTTGGCAGACG ENSP00000399168.2:p.Met122LeufsTer20
ENST00000434333.1:c.396_397insTTGGCAGACG ENSP00000405931.1:p.Met133LeufsTer20
ENST00000474381.1:n.238_239insTTGGCAGACG
ENST00000498007.1:n.629_630insTTGGCAGACG
NM_005514.6:c.363_364insTTGGCAGACG NP_005505.2:p.Met122LeufsTer20
XM_011514556.1:c.396_397insTTGGCAGACG XP_011512858.1:p.Met133LeufsTer20
XM_011514557.1:c.363_364insTTGGCAGACG XP_011512859.1:p.Met122LeufsTer20
XR_926175.1:n.373_374insTTGGCAGACG
NM_005514.7:c.363_364insTTGGCAGACG NP_005505.2:p.Met122LeufsTer20
NM_005514.8:c.363_364insTTGGCAGACG MANE Select NP_005505.2:p.Met122LeufsTer20