Canonical Allele Identifier: CA2679055068

Gene: RHAG

Linked Data

• gnomAD v4: 6-49636843-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49636843A>G , CM000668.2:g.49636843A>G	GRCh38
NC_000006.11:g.49604556A>G , CM000668.1:g.49604556A>G	GRCh37
NC_000006.10:g.49712515A>G	NCBI36
NG_011704.1:g.5032T>C

Transcript Alleles

HGVS	Amino-acid change
NM_000324.2:c.-31T>C	NP_000315.2:n.-31T>C
XM_011514788.1:c.-31T>C	XP_011513090.1:n.-31T>C