Canonical Allele Identifier: CA364402978

Gene: RHAG

Linked Data

• dbSNP Id: rs1472966427
• gnomAD v2: 6-49586928-T-C
• gnomAD v3: 6-49619215-T-C
• gnomAD v4: 6-49619215-T-C
• MyVariant Identifiers: chr6:g.49586928T>C (hg19) ; chr6:g.49619215T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619215T>C , CM000668.2:g.49619215T>C	GRCh38
NC_000006.11:g.49586928T>C , CM000668.1:g.49586928T>C	GRCh37
NC_000006.10:g.49694887T>C	NCBI36
NG_011704.1:g.22660A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.305A>G MANE Select	ENSP00000360217.4:p.Gln102Arg
ENST00000642530.1:n.580A>G
ENST00000646272.1:c.305A>G	ENSP00000494337.1:p.Gln102Arg
ENST00000646939.1:c.305A>G	ENSP00000494709.1:p.Gln102Arg
ENST00000646963.1:c.305A>G	ENSP00000495337.1:p.Gln102Arg
ENST00000229810.9:c.305A>G	ENSP00000229810.8:p.Gln102Arg
ENST00000371175.8:c.305A>G	ENSP00000360217.4:p.Gln102Arg
ENST00000618248.3:c.305A>G	ENSP00000482984.1:p.Gln102Arg
NM_000324.2:c.305A>G	NP_000315.2:p.Gln102Arg
XM_011514788.1:c.305A>G	XP_011513090.1:p.Gln102Arg
NM_000324.3:c.305A>G MANE Select	NP_000315.2:p.Gln102Arg