Canonical Allele Identifier: CA1215986958
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192812276C= , CM000663.2:g.192812276C= GRCh38
NC_000001.10:g.192781406C= , CM000663.1:g.192781406C= GRCh37
NC_000001.9:g.191048029C= NCBI36
NG_012800.1:g.8238C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.6:c.*680C= ENSP00000235382.5:n.*680C=
NM_002923.3:c.*680C= NP_002914.1:n.*680C=