Canonical Allele Identifier: CA1088821926
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs1763017860
gnomAD v3: 6-49636842-G-A
gnomAD v4: 6-49636842-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636842G>A , CM000668.2:g.49636842G>A GRCh38
NC_000006.11:g.49604555G>A , CM000668.1:g.49604555G>A GRCh37
NC_000006.10:g.49712514G>A NCBI36
NG_011704.1:g.5033C>T

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-30C>T NP_000315.2:n.-30C>T
XM_011514788.1:c.-30C>T XP_011513090.1:n.-30C>T