Canonical Allele Identifier: CA1619117532

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354644G= , CM000668.2:g.31354644G=	GRCh38
NC_000006.11:g.31322421G= , CM000668.1:g.31322421G=	GRCh37
NC_000006.10:g.31430400G=	NCBI36
NG_023187.1:g.7569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3081C=
ENST00000481849.6:n.3041C=
ENST00000497377.6:n.2948C=
ENST00000640094.2:c.917C=	ENSP00000491275.2:p.Ser306=
ENST00000696558.1:c.1103C=	ENSP00000512716.1:n.1103C=
ENST00000696559.1:c.1034C=	ENSP00000512717.1:p.Ser345=
ENST00000696560.1:c.1034C=	ENSP00000512718.1:p.Ser345=
ENST00000696561.1:c.1034C=	ENSP00000512719.1:p.Ser345=
ENST00000696562.1:c.1034C=	ENSP00000512720.1:p.Ser345=
ENST00000412585.7:c.1034C= MANE Select	ENSP00000399168.2:p.Ser345=
ENST00000640094.1:c.110C=	ENSP00000491275.1:p.Ser37=
ENST00000412585.6:c.1034C=	ENSP00000399168.2:p.Ser345=
ENST00000481849.5:n.163C=
ENST00000497377.5:n.433C=
NM_005514.6:c.1034C=	NP_005505.2:p.Ser345=
XM_011514556.1:c.1067C=	XP_011512858.1:p.Ser356=
XM_011514557.1:c.917C=	XP_011512859.1:p.Ser306=
XR_926175.1:n.1473C=
NM_005514.7:c.1034C=	NP_005505.2:p.Ser345=
NM_005514.8:c.1034C= MANE Select	NP_005505.2:p.Ser345=