Canonical Allele Identifier: CA136831291
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs879124740
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354138_31354139insC , CM000668.2:g.31354138_31354139insC GRCh38
NC_000006.11:g.31321915_31321916insC , CM000668.1:g.31321915_31321916insC GRCh37
NC_000006.10:g.31429894_31429895insC NCBI36
NG_023187.1:g.8074_8075insG

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3298_3299insG
ENST00000481849.6:n.3258_3259insG
ENST00000497377.6:n.3165_3166insG
ENST00000696558.1:c.1320_1321insG ENSP00000512716.1:n.1320_1321insG
ENST00000696559.1:c.*162_*163insG ENSP00000512717.1:n.*162_*163insG
ENST00000696560.1:c.*162_*163insG ENSP00000512718.1:n.*162_*163insG
ENST00000696561.1:c.*162_*163insG ENSP00000512719.1:n.*162_*163insG
ENST00000696562.1:c.*162_*163insG ENSP00000512720.1:n.*162_*163insG
ENST00000412585.7:c.*162_*163insG MANE Select ENSP00000399168.2:n.*162_*163insG
ENST00000412585.6:c.*162_*163insG ENSP00000399168.2:n.*162_*163insG
ENST00000481849.5:n.486_487insG
ENST00000497377.5:n.650_651insG
NM_005514.6:c.*162_*163insG NP_005505.2:n.*162_*163insG
XM_011514556.1:c.*162_*163insG XP_011512858.1:n.*162_*163insG
XM_011514557.1:c.*162_*163insG XP_011512859.1:n.*162_*163insG
XR_926175.1:n.1690_1691insG
NM_005514.7:c.*162_*163insG NP_005505.2:n.*162_*163insG
NM_005514.8:c.*162_*163insG MANE Select NP_005505.2:n.*162_*163insG
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