Canonical Allele Identifier: CA1619118784

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355389A= , CM000668.2:g.31355389A=	GRCh38
NC_000006.11:g.31323166A= , CM000668.1:g.31323166A=	GRCh37
NC_000006.10:g.31431145A=	NCBI36
NG_023187.1:g.6824T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2870T=
ENST00000481849.6:n.2296T=
ENST00000497377.6:n.2296T=
ENST00000640094.2:c.823T=	ENSP00000491275.2:p.Ser275=
ENST00000696558.1:c.892T=	ENSP00000512716.1:n.892T=
ENST00000696559.1:c.823T=	ENSP00000512717.1:p.Ser275=
ENST00000696560.1:c.823T=	ENSP00000512718.1:p.Ser275=
ENST00000696561.1:c.823T=	ENSP00000512719.1:p.Ser275=
ENST00000696562.1:c.823T=	ENSP00000512720.1:p.Ser275=
ENST00000412585.7:c.823T= MANE Select	ENSP00000399168.2:p.Ser275=
ENST00000640094.1:c.16T=	ENSP00000491275.1:p.Ser6=
ENST00000412585.6:c.823T=	ENSP00000399168.2:p.Ser275=
ENST00000463574.1:n.414T=
NM_005514.6:c.823T=	NP_005505.2:p.Ser275=
XM_011514556.1:c.856T=	XP_011512858.1:p.Ser286=
XM_011514557.1:c.823T=	XP_011512859.1:p.Ser275=
XR_926175.1:n.1262T=
NM_005514.7:c.823T=	NP_005505.2:p.Ser275=
NM_005514.8:c.823T= MANE Select	NP_005505.2:p.Ser275=