Canonical Allele Identifier: CA646208665
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812281G>C , CM000663.2:g.192812281G>C GRCh38
NC_000001.10:g.192781411G>C , CM000663.1:g.192781411G>C GRCh37
NC_000001.9:g.191048034G>C NCBI36
NG_012800.1:g.8243G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.6:c.*685G>C ENSP00000235382.5:n.*685G>C