Canonical Allele Identifier: CA1215986764
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs767891880

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811799T>C , CM000663.2:g.192811799T>C GRCh38
NC_000001.10:g.192780929T>C , CM000663.1:g.192780929T>C GRCh37
NC_000001.9:g.191047552T>C NCBI36
NG_012800.1:g.7761T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*203T>C MANE Select ENSP00000235382.5:n.*203T>C
ENST00000235382.6:c.*203T>C ENSP00000235382.5:n.*203T>C
NM_002923.3:c.*203T>C NP_002914.1:n.*203T>C
NM_002923.4:c.*203T>C MANE Select NP_002914.1:n.*203T>C