Canonical Allele Identifier: CA1619117903

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354955A= , CM000668.2:g.31354955A=	GRCh38
NC_000006.11:g.31322732A= , CM000668.1:g.31322732A=	GRCh37
NC_000006.10:g.31430711A=	NCBI36
NG_023187.1:g.7258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+152T=
ENST00000481849.6:n.2730T=
ENST00000497377.6:n.2637T=
ENST00000640094.2:c.896-290T=	ENSP00000491275.2:n.896-290T=
ENST00000696558.1:c.1081+152T=	ENSP00000512716.1:n.1081+152T=
ENST00000696559.1:c.1012+152T=	ENSP00000512717.1:n.1012+152T=
ENST00000696560.1:c.1012+152T=	ENSP00000512718.1:n.1012+152T=
ENST00000696561.1:c.1012+152T=	ENSP00000512719.1:n.1012+152T=
ENST00000696562.1:c.1012+152T=	ENSP00000512720.1:n.1012+152T=
ENST00000412585.7:c.1012+152T= MANE Select	ENSP00000399168.2:n.1012+152T=
ENST00000640094.1:c.89-290T=	ENSP00000491275.1:n.89-290T=
ENST00000412585.6:c.1012+152T=	ENSP00000399168.2:n.1012+152T=
ENST00000497377.5:n.122T=
NM_005514.6:c.1012+152T=	NP_005505.2:n.1012+152T=
XM_011514556.1:c.1045+152T=	XP_011512858.1:n.1045+152T=
XM_011514557.1:c.896-290T=	XP_011512859.1:n.896-290T=
XR_926175.1:n.1451+152T=
NM_005514.7:c.1012+152T=	NP_005505.2:n.1012+152T=
NM_005514.8:c.1012+152T= MANE Select	NP_005505.2:n.1012+152T=