Canonical Allele Identifier: CA364398146

Gene: RHAG

Linked Data

• dbSNP Id: rs1304780034
• gnomAD v2: 6-49580124-A-G
• gnomAD v4: 6-49612411-A-G
• MyVariant Identifiers: chr6:g.49580124A>G (hg19) ; chr6:g.49612411A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612411A>G , CM000668.2:g.49612411A>G	GRCh38
NC_000006.11:g.49580124A>G , CM000668.1:g.49580124A>G	GRCh37
NC_000006.10:g.49688083A>G	NCBI36
NG_011704.1:g.29464T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.931T>C MANE Select	ENSP00000360217.4:p.Tyr311His
ENST00000646272.1:c.931T>C	ENSP00000494337.1:p.Tyr311His
ENST00000646874.1:n.621T>C
ENST00000646939.1:c.931T>C	ENSP00000494709.1:p.Tyr311His
ENST00000646963.1:c.931T>C	ENSP00000495337.1:p.Tyr311His
ENST00000229810.9:c.931T>C	ENSP00000229810.8:p.Tyr311His
ENST00000371175.8:c.931T>C	ENSP00000360217.4:p.Tyr311His
ENST00000618248.3:c.931T>C	ENSP00000482984.1:p.Tyr311His
NM_000324.2:c.931T>C	NP_000315.2:p.Tyr311His
NM_000324.3:c.931T>C MANE Select	NP_000315.2:p.Tyr311His