Canonical Allele Identifier: CA1010583447

Gene: RGS2

Linked Data

• dbSNP Id: rs1665605634
• gnomAD v3: 1-192812280-T-C
• gnomAD v4: 1-192812280-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812280T>C , CM000663.2:g.192812280T>C	GRCh38
NC_000001.10:g.192781410T>C , CM000663.1:g.192781410T>C	GRCh37
NC_000001.9:g.191048033T>C	NCBI36
NG_012800.1:g.8242T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.6:c.*684T>C	ENSP00000235382.5:n.*684T>C