Canonical Allele Identifier: CA1619118728

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355357T= , CM000668.2:g.31355357T=	GRCh38
NC_000006.11:g.31323134T= , CM000668.1:g.31323134T=	GRCh37
NC_000006.10:g.31431113T=	NCBI36
NG_023187.1:g.6856A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005514.8:c.855A= MANE Select	NP_005505.2:p.Val285=
ENST00000412585.7:c.855A= MANE Select	ENSP00000399168.2:p.Val285=
NM_005514.6:c.855A=	NP_005505.2:p.Val285=
NM_005514.7:c.855A=	NP_005505.2:p.Val285=
ENST00000412585.6:c.855A=	ENSP00000399168.2:p.Val285=
ENST00000463574.1:n.446A=
ENST00000474381.2:n.2902A=
ENST00000481849.6:n.2328A=
ENST00000497377.6:n.2328A=
ENST00000640094.1:c.48A=	ENSP00000491275.1:p.Val16=
ENST00000640094.2:c.855A=	ENSP00000491275.2:p.Val285=
ENST00000696558.1:c.924A=	ENSP00000512716.1:n.924A=
ENST00000696559.1:c.855A=	ENSP00000512717.1:p.Val285=
ENST00000696560.1:c.855A=	ENSP00000512718.1:p.Val285=
ENST00000696561.1:c.855A=	ENSP00000512719.1:p.Val285=
ENST00000696562.1:c.855A=	ENSP00000512720.1:p.Val285=
XM_011514556.1:c.888A=	XP_011512858.1:p.Val296=
XM_011514557.1:c.855A=	XP_011512859.1:p.Val285=
XR_926175.1:n.1294A=