Canonical Allele Identifier: CA35070366
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs775814329

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811841T>C , CM000663.2:g.192811841T>C GRCh38
NC_000001.10:g.192780971T>C , CM000663.1:g.192780971T>C GRCh37
NC_000001.9:g.191047594T>C NCBI36
NG_012800.1:g.7803T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*245T>C MANE Select ENSP00000235382.5:n.*245T>C
ENST00000235382.6:c.*245T>C ENSP00000235382.5:n.*245T>C
NM_002923.3:c.*245T>C NP_002914.1:n.*245T>C
NM_002923.4:c.*245T>C MANE Select NP_002914.1:n.*245T>C