Canonical Allele Identifier: CA1619116454

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354070T= , CM000668.2:g.31354070T=	GRCh38
NC_000006.11:g.31321847T= , CM000668.1:g.31321847T=	GRCh37
NC_000006.10:g.31429826T=	NCBI36
NG_023187.1:g.8143A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3367A=
ENST00000481849.6:n.3327A=
ENST00000497377.6:n.3234A=
ENST00000696558.1:c.1389A=	ENSP00000512716.1:n.1389A=
ENST00000696559.1:c.*231A=	ENSP00000512717.1:n.*231A=
ENST00000696560.1:c.*231A=	ENSP00000512718.1:n.*231A=
ENST00000696561.1:c.*231A=	ENSP00000512719.1:n.*231A=
ENST00000696562.1:c.*231A=	ENSP00000512720.1:n.*231A=
ENST00000412585.7:c.*231A= MANE Select	ENSP00000399168.2:n.*231A=
ENST00000412585.6:c.*231A=	ENSP00000399168.2:n.*231A=
ENST00000481849.5:n.555A=
ENST00000497377.5:n.719A=
NM_005514.6:c.*231A=	NP_005505.2:n.*231A=
XM_011514556.1:c.*231A=	XP_011512858.1:n.*231A=
XM_011514557.1:c.*231A=	XP_011512859.1:n.*231A=
XR_926175.1:n.1759A=
NM_005514.7:c.*231A=	NP_005505.2:n.*231A=
NM_005514.8:c.*231A= MANE Select	NP_005505.2:n.*231A=