Canonical Allele Identifier: CA1627478013

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619344A= , CM000668.2:g.49619344A=	GRCh38
NC_000006.11:g.49587057A= , CM000668.1:g.49587057A=	GRCh37
NC_000006.10:g.49695016A=	NCBI36
NG_011704.1:g.22531T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.176T= MANE Select	ENSP00000360217.4:p.Val59=
ENST00000642530.1:n.451T=
ENST00000646272.1:c.176T=	ENSP00000494337.1:p.Val59=
ENST00000646939.1:c.176T=	ENSP00000494709.1:p.Val59=
ENST00000646963.1:c.176T=	ENSP00000495337.1:p.Val59=
ENST00000229810.9:c.176T=	ENSP00000229810.8:p.Val59=
ENST00000371175.8:c.176T=	ENSP00000360217.4:p.Val59=
ENST00000618248.3:c.176T=	ENSP00000482984.1:p.Val59=
NM_000324.2:c.176T=	NP_000315.2:p.Val59=
XM_011514788.1:c.176T=	XP_011513090.1:p.Val59=
NM_000324.3:c.176T= MANE Select	NP_000315.2:p.Val59=