Canonical Allele Identifier: CA825500489

Gene: RHAG

Linked Data

• dbSNP Id: rs562347902
• gnomAD v3: 6-49636856-G-C
• gnomAD v4: 6-49636856-G-C
• MyVariant Identifiers: chr6:g.49604569G>C (hg19) ; chr6:g.49636856G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49636856G>C , CM000668.2:g.49636856G>C	GRCh38
NC_000006.11:g.49604569G>C , CM000668.1:g.49604569G>C	GRCh37
NC_000006.10:g.49712528G>C	NCBI36
NG_011704.1:g.5019C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000324.2:c.-44C>G	NP_000315.2:n.-44C>G
XM_011514788.1:c.-44C>G	XP_011513090.1:n.-44C>G