Canonical Allele Identifier: CA1627469194

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612506C= , CM000668.2:g.49612506C=	GRCh38
NC_000006.11:g.49580219C= , CM000668.1:g.49580219C=	GRCh37
NC_000006.10:g.49688178C=	NCBI36
NG_011704.1:g.29369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.836G= MANE Select	ENSP00000360217.4:p.Gly279=
ENST00000646272.1:c.836G=	ENSP00000494337.1:p.Gly279=
ENST00000646874.1:n.526G=
ENST00000646939.1:c.836G=	ENSP00000494709.1:p.Gly279=
ENST00000646963.1:c.836G=	ENSP00000495337.1:p.Gly279=
ENST00000229810.9:c.836G=	ENSP00000229810.8:p.Gly279=
ENST00000371175.8:c.836G=	ENSP00000360217.4:p.Gly279=
ENST00000618248.3:c.836G=	ENSP00000482984.1:p.Gly279=
NM_000324.2:c.836G=	NP_000315.2:p.Gly279=
NM_000324.3:c.836G= MANE Select	NP_000315.2:p.Gly279=