Canonical Allele Identifier: CA1619116470

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354092G= , CM000668.2:g.31354092G=	GRCh38
NC_000006.11:g.31321869G= , CM000668.1:g.31321869G=	GRCh37
NC_000006.10:g.31429848G=	NCBI36
NG_023187.1:g.8121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3345C=
ENST00000481849.6:n.3305C=
ENST00000497377.6:n.3212C=
ENST00000696558.1:c.1367C=	ENSP00000512716.1:n.1367C=
ENST00000696559.1:c.*209C=	ENSP00000512717.1:n.*209C=
ENST00000696560.1:c.*209C=	ENSP00000512718.1:n.*209C=
ENST00000696561.1:c.*209C=	ENSP00000512719.1:n.*209C=
ENST00000696562.1:c.*209C=	ENSP00000512720.1:n.*209C=
ENST00000412585.7:c.*209C= MANE Select	ENSP00000399168.2:n.*209C=
ENST00000412585.6:c.*209C=	ENSP00000399168.2:n.*209C=
ENST00000481849.5:n.533C=
ENST00000497377.5:n.697C=
NM_005514.6:c.*209C=	NP_005505.2:n.*209C=
XM_011514556.1:c.*209C=	XP_011512858.1:n.*209C=
XM_011514557.1:c.*209C=	XP_011512859.1:n.*209C=
XR_926175.1:n.1737C=
NM_005514.7:c.*209C=	NP_005505.2:n.*209C=
NM_005514.8:c.*209C= MANE Select	NP_005505.2:n.*209C=