Canonical Allele Identifier: CA1619118375

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355208G= , CM000668.2:g.31355208G=	GRCh38
NC_000006.11:g.31322985G= , CM000668.1:g.31322985G=	GRCh37
NC_000006.10:g.31430964G=	NCBI36
NG_023187.1:g.7005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2958C=
ENST00000481849.6:n.2477C=
ENST00000497377.6:n.2384C=
ENST00000640094.2:c.895+109C=	ENSP00000491275.2:n.895+109C=
ENST00000696558.1:c.980C=	ENSP00000512716.1:n.980C=
ENST00000696559.1:c.911C=	ENSP00000512717.1:p.Ser304=
ENST00000696560.1:c.911C=	ENSP00000512718.1:p.Ser304=
ENST00000696561.1:c.911C=	ENSP00000512719.1:p.Ser304=
ENST00000696562.1:c.911C=	ENSP00000512720.1:p.Ser304=
ENST00000412585.7:c.911C= MANE Select	ENSP00000399168.2:p.Ser304=
ENST00000640094.1:c.88+109C=	ENSP00000491275.1:n.88+109C=
ENST00000412585.6:c.911C=	ENSP00000399168.2:p.Ser304=
ENST00000463574.1:n.502C=
NM_005514.6:c.911C=	NP_005505.2:p.Ser304=
XM_011514556.1:c.944C=	XP_011512858.1:p.Ser315=
XM_011514557.1:c.895+109C=	XP_011512859.1:n.895+109C=
XR_926175.1:n.1350C=
NM_005514.7:c.911C=	NP_005505.2:p.Ser304=
NM_005514.8:c.911C= MANE Select	NP_005505.2:p.Ser304=