Canonical Allele Identifier: CA1627469216

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612518G= , CM000668.2:g.49612518G=	GRCh38
NC_000006.11:g.49580231G= , CM000668.1:g.49580231G=	GRCh37
NC_000006.10:g.49688190G=	NCBI36
NG_011704.1:g.29357C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.824C= MANE Select	ENSP00000360217.4:p.Ala275=
ENST00000646272.1:c.824C=	ENSP00000494337.1:p.Ala275=
ENST00000646874.1:n.514C=
ENST00000646939.1:c.824C=	ENSP00000494709.1:p.Ala275=
ENST00000646963.1:c.824C=	ENSP00000495337.1:p.Ala275=
ENST00000229810.9:c.824C=	ENSP00000229810.8:p.Ala275=
ENST00000371175.8:c.824C=	ENSP00000360217.4:p.Ala275=
ENST00000618248.3:c.824C=	ENSP00000482984.1:p.Ala275=
NM_000324.2:c.824C=	NP_000315.2:p.Ala275=
NM_000324.3:c.824C= MANE Select	NP_000315.2:p.Ala275=