Canonical Allele Identifier: CA1627468965

Gene: RHAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612415A= , CM000668.2:g.49612415A=	GRCh38
NC_000006.11:g.49580128A= , CM000668.1:g.49580128A=	GRCh37
NC_000006.10:g.49688087A=	NCBI36
NG_011704.1:g.29460T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.927T= MANE Select	ENSP00000360217.4:p.Leu309=
ENST00000646272.1:c.927T=	ENSP00000494337.1:p.Leu309=
ENST00000646874.1:n.617T=
ENST00000646939.1:c.927T=	ENSP00000494709.1:p.Leu309=
ENST00000646963.1:c.927T=	ENSP00000495337.1:p.Leu309=
ENST00000229810.9:c.927T=	ENSP00000229810.8:p.Leu309=
ENST00000371175.8:c.927T=	ENSP00000360217.4:p.Leu309=
ENST00000618248.3:c.927T=	ENSP00000482984.1:p.Leu309=
NM_000324.2:c.927T=	NP_000315.2:p.Leu309=
NM_000324.3:c.927T= MANE Select	NP_000315.2:p.Leu309=