Canonical Allele Identifier: CA1215986961
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665605560

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812279T>A , CM000663.2:g.192812279T>A GRCh38
NC_000001.10:g.192781409T>A , CM000663.1:g.192781409T>A GRCh37
NC_000001.9:g.191048032T>A NCBI36
NG_012800.1:g.8241T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.6:c.*683T>A ENSP00000235382.5:n.*683T>A