Canonical Allele Identifier: CA567156164

Gene: RHAG

Linked Data

• dbSNP Id: rs1402303391
• gnomAD v2: 6-49586845-T-C
• gnomAD v4: 6-49619132-T-C
• MyVariant Identifiers: chr6:g.49586845T>C (hg19) ; chr6:g.49619132T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619132T>C , CM000668.2:g.49619132T>C	GRCh38
NC_000006.11:g.49586845T>C , CM000668.1:g.49586845T>C	GRCh37
NC_000006.10:g.49694804T>C	NCBI36
NG_011704.1:g.22743A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+47A>G MANE Select	ENSP00000360217.4:n.341+47A>G
ENST00000642530.1:n.616+47A>G
ENST00000646272.1:c.341+47A>G	ENSP00000494337.1:n.341+47A>G
ENST00000646939.1:c.341+47A>G	ENSP00000494709.1:n.341+47A>G
ENST00000646963.1:c.341+47A>G	ENSP00000495337.1:n.341+47A>G
ENST00000229810.9:c.341+47A>G	ENSP00000229810.8:n.341+47A>G
ENST00000371175.8:c.341+47A>G	ENSP00000360217.4:n.341+47A>G
ENST00000618248.3:c.341+47A>G	ENSP00000482984.1:n.341+47A>G
NM_000324.2:c.341+47A>G	NP_000315.2:n.341+47A>G
XM_011514788.1:c.341+47A>G	XP_011513090.1:n.341+47A>G
NM_000324.3:c.341+47A>G MANE Select	NP_000315.2:n.341+47A>G