Canonical Allele Identifier: CA136831300
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs386699122
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354139_31354142delinsCAGT , CM000668.2:g.31354139_31354142delinsCAGT GRCh38
NC_000006.11:g.31321916_31321919delinsCAGT , CM000668.1:g.31321916_31321919delinsCAGT GRCh37
NC_000006.10:g.31429895_31429898delinsCAGT NCBI36
NG_023187.1:g.8071_8074delinsACTG

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3295_3298delinsACTG
ENST00000481849.6:n.3255_3258delinsACTG
ENST00000497377.6:n.3162_3165delinsACTG
ENST00000696558.1:c.1317_1320delinsACTG ENSP00000512716.1:n.1317_1320delinsACTG
ENST00000696559.1:c.*159_*162delinsACTG ENSP00000512717.1:n.*159_*162delinsACTG
ENST00000696560.1:c.*159_*162delinsACTG ENSP00000512718.1:n.*159_*162delinsACTG
ENST00000696561.1:c.*159_*162delinsACTG ENSP00000512719.1:n.*159_*162delinsACTG
ENST00000696562.1:c.*159_*162delinsACTG ENSP00000512720.1:n.*159_*162delinsACTG
ENST00000412585.7:c.*159_*162delinsACTG MANE Select ENSP00000399168.2:n.*159_*162delinsACTG
ENST00000412585.6:c.*159_*162delinsACTG ENSP00000399168.2:n.*159_*162delinsACTG
ENST00000481849.5:n.483_486delinsACTG
ENST00000497377.5:n.647_650delinsACTG
NM_005514.6:c.*159_*162delinsACTG NP_005505.2:n.*159_*162delinsACTG
XM_011514556.1:c.*159_*162delinsACTG XP_011512858.1:n.*159_*162delinsACTG
XM_011514557.1:c.*159_*162delinsACTG XP_011512859.1:n.*159_*162delinsACTG
XR_926175.1:n.1687_1690delinsACTG
NM_005514.7:c.*159_*162delinsACTG NP_005505.2:n.*159_*162delinsACTG
NM_005514.8:c.*159_*162delinsACTG MANE Select NP_005505.2:n.*159_*162delinsACTG
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