Canonical Allele Identifier: CA1627461169

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49606921C= , CM000668.2:g.49606921C=	GRCh38
NC_000006.11:g.49574634C= , CM000668.1:g.49574634C=	GRCh37
NC_000006.10:g.49682593C=	NCBI36
NG_011704.1:g.34954G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000324.3:c.1139G= MANE Select	NP_000315.2:p.Gly380=
ENST00000371175.10:c.1139G= MANE Select	ENSP00000360217.4:p.Gly380=
NM_000324.2:c.1139G=	NP_000315.2:p.Gly380=
ENST00000229810.9:c.1139G=	ENSP00000229810.8:p.Gly380=
ENST00000371175.8:c.1139G=	ENSP00000360217.4:p.Gly380=
ENST00000618248.3:c.1138+229G=	ENSP00000482984.1:n.1138+229G=
ENST00000646272.1:c.1139G=	ENSP00000494337.1:p.Gly380=
ENST00000646939.1:c.1017G=	ENSP00000494709.1:p.Arg339=
ENST00000646963.1:c.1138+229G=	ENSP00000495337.1:n.1138+229G=