Canonical Allele Identifier: CA1619116553

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354222G= , CM000668.2:g.31354222G=	GRCh38
NC_000006.11:g.31321999G= , CM000668.1:g.31321999G=	GRCh37
NC_000006.10:g.31429978G=	NCBI36
NG_023187.1:g.7991C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3215C=
ENST00000481849.6:n.3175C=
ENST00000497377.6:n.3082C=
ENST00000696558.1:c.1237C=	ENSP00000512716.1:n.1237C=
ENST00000696559.1:c.*79C=	ENSP00000512717.1:n.*79C=
ENST00000696560.1:c.*79C=	ENSP00000512718.1:n.*79C=
ENST00000696561.1:c.*79C=	ENSP00000512719.1:n.*79C=
ENST00000696562.1:c.*79C=	ENSP00000512720.1:n.*79C=
ENST00000412585.7:c.*79C= MANE Select	ENSP00000399168.2:n.*79C=
ENST00000412585.6:c.*79C=	ENSP00000399168.2:n.*79C=
ENST00000481849.5:n.403C=
ENST00000497377.5:n.567C=
NM_005514.6:c.*79C=	NP_005505.2:n.*79C=
XM_011514556.1:c.*79C=	XP_011512858.1:n.*79C=
XM_011514557.1:c.*79C=	XP_011512859.1:n.*79C=
XR_926175.1:n.1607C=
NM_005514.7:c.*79C=	NP_005505.2:n.*79C=
NM_005514.8:c.*79C= MANE Select	NP_005505.2:n.*79C=