Canonical Allele Identifier: CA1627456301

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49636836C= , CM000668.2:g.49636836C=	GRCh38
NC_000006.11:g.49604549C= , CM000668.1:g.49604549C=	GRCh37
NC_000006.10:g.49712508C=	NCBI36
NG_011704.1:g.5039G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.-24G= MANE Select	ENSP00000360217.4:n.-24G=
ENST00000642530.1:n.4G=
ENST00000646272.1:c.-24G=	ENSP00000494337.1:n.-24G=
ENST00000646939.1:c.-24G=	ENSP00000494709.1:n.-24G=
ENST00000646963.1:c.-24G=	ENSP00000495337.1:n.-24G=
ENST00000229810.9:c.-24G=	ENSP00000229810.8:n.-24G=
ENST00000371175.8:c.-24G=	ENSP00000360217.4:n.-24G=
ENST00000618248.3:c.-24G=	ENSP00000482984.1:n.-24G=
NM_000324.2:c.-24G=	NP_000315.2:n.-24G=
XM_011514788.1:c.-24G=	XP_011513090.1:n.-24G=
NM_000324.3:c.-24G= MANE Select	NP_000315.2:n.-24G=