Canonical Allele Identifier: CA1627478015

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619346A= , CM000668.2:g.49619346A=	GRCh38
NC_000006.11:g.49587059A= , CM000668.1:g.49587059A=	GRCh37
NC_000006.10:g.49695018A=	NCBI36
NG_011704.1:g.22529T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.174T= MANE Select	ENSP00000360217.4:p.His58=
ENST00000642530.1:n.449T=
ENST00000646272.1:c.174T=	ENSP00000494337.1:p.His58=
ENST00000646939.1:c.174T=	ENSP00000494709.1:p.His58=
ENST00000646963.1:c.174T=	ENSP00000495337.1:p.His58=
ENST00000229810.9:c.174T=	ENSP00000229810.8:p.His58=
ENST00000371175.8:c.174T=	ENSP00000360217.4:p.His58=
ENST00000618248.3:c.174T=	ENSP00000482984.1:p.His58=
NM_000324.2:c.174T=	NP_000315.2:p.His58=
XM_011514788.1:c.174T=	XP_011513090.1:p.His58=
NM_000324.3:c.174T= MANE Select	NP_000315.2:p.His58=