Canonical Allele Identifier: CA917712164
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1554209581
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354139_31354140delinsCA , CM000668.2:g.31354139_31354140delinsCA GRCh38
NC_000006.11:g.31321916_31321917delinsCA , CM000668.1:g.31321916_31321917delinsCA GRCh37
NC_000006.10:g.31429895_31429896delinsCA NCBI36
NG_023187.1:g.8073_8074delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3297_3298delinsTG
ENST00000481849.6:n.3257_3258delinsTG
ENST00000497377.6:n.3164_3165delinsTG
ENST00000696558.1:c.1319_1320delinsTG ENSP00000512716.1:n.1319_1320delinsTG
ENST00000696559.1:c.*161_*162delinsTG ENSP00000512717.1:n.*161_*162delinsTG
ENST00000696560.1:c.*161_*162delinsTG ENSP00000512718.1:n.*161_*162delinsTG
ENST00000696561.1:c.*161_*162delinsTG ENSP00000512719.1:n.*161_*162delinsTG
ENST00000696562.1:c.*161_*162delinsTG ENSP00000512720.1:n.*161_*162delinsTG
ENST00000412585.7:c.*161_*162delinsTG MANE Select ENSP00000399168.2:n.*161_*162delinsTG
ENST00000412585.6:c.*161_*162delinsTG ENSP00000399168.2:n.*161_*162delinsTG
ENST00000481849.5:n.485_486delinsTG
ENST00000497377.5:n.649_650delinsTG
NM_005514.6:c.*161_*162delinsTG NP_005505.2:n.*161_*162delinsTG
XM_011514556.1:c.*161_*162delinsTG XP_011512858.1:n.*161_*162delinsTG
XM_011514557.1:c.*161_*162delinsTG XP_011512859.1:n.*161_*162delinsTG
XR_926175.1:n.1689_1690delinsTG
NM_005514.7:c.*161_*162delinsTG NP_005505.2:n.*161_*162delinsTG
NM_005514.8:c.*161_*162delinsTG MANE Select NP_005505.2:n.*161_*162delinsTG
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