Canonical Allele Identifier: CA3711656
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs761351954

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356469_31356470insC , CM000668.2:g.31356469_31356470insC GRCh38
NC_000006.11:g.31324246_31324247insC , CM000668.1:g.31324246_31324247insC GRCh37
NC_000006.10:g.31432225_31432226insC NCBI36
NG_023187.1:g.5743_5744insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-28_1817-27insG
ENST00000481849.6:n.1817-28_1817-27insG
ENST00000497377.6:n.1817-28_1817-27insG
ENST00000640094.2:c.344-28_344-27insG ENSP00000491275.2:n.344-28_344-27insG
ENST00000696558.1:c.344-28_344-27insG ENSP00000512716.1:n.344-28_344-27insG
ENST00000696559.1:c.344-28_344-27insG ENSP00000512717.1:n.344-28_344-27insG
ENST00000696560.1:c.344-28_344-27insG ENSP00000512718.1:n.344-28_344-27insG
ENST00000696561.1:c.344-28_344-27insG ENSP00000512719.1:n.344-28_344-27insG
ENST00000696562.1:c.344-28_344-27insG ENSP00000512720.1:n.344-28_344-27insG
ENST00000412585.7:c.344-28_344-27insG MANE Select ENSP00000399168.2:n.344-28_344-27insG
ENST00000412585.6:c.344-28_344-27insG ENSP00000399168.2:n.344-28_344-27insG
ENST00000434333.1:c.377-28_377-27insG ENSP00000405931.1:n.377-28_377-27insG
ENST00000474381.1:n.219-28_219-27insG
ENST00000498007.1:n.582_583insG
NM_005514.6:c.344-28_344-27insG NP_005505.2:n.344-28_344-27insG
XM_011514556.1:c.377-28_377-27insG XP_011512858.1:n.377-28_377-27insG
XM_011514557.1:c.344-28_344-27insG XP_011512859.1:n.344-28_344-27insG
XR_926175.1:n.354-28_354-27insG
NM_005514.7:c.344-28_344-27insG NP_005505.2:n.344-28_344-27insG
NM_005514.8:c.344-28_344-27insG MANE Select NP_005505.2:n.344-28_344-27insG