Canonical Allele Identifier: CA364398545

Gene: RHAG

Linked Data

• dbSNP Id: rs121918587
• MyVariant Identifiers: chr6:g.49580219C>G (hg19) ; chr6:g.49612506C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.836G>C MANE Select	ENSP00000360217.4:p.Gly279Ala
ENST00000646272.1:c.836G>C	ENSP00000494337.1:p.Gly279Ala
ENST00000646874.1:n.526G>C
ENST00000646939.1:c.836G>C	ENSP00000494709.1:p.Gly279Ala
ENST00000646963.1:c.836G>C	ENSP00000495337.1:p.Gly279Ala
ENST00000229810.9:c.836G>C	ENSP00000229810.8:p.Gly279Ala
ENST00000371175.8:c.836G>C	ENSP00000360217.4:p.Gly279Ala
ENST00000618248.3:c.836G>C	ENSP00000482984.1:p.Gly279Ala
NM_000324.2:c.836G>C	NP_000315.2:p.Gly279Ala
NM_000324.3:c.836G>C MANE Select	NP_000315.2:p.Gly279Ala