Canonical Allele Identifier: CA1215986706
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811641C= , CM000663.2:g.192811641C= GRCh38
NC_000001.10:g.192780771C= , CM000663.1:g.192780771C= GRCh37
NC_000001.9:g.191047394C= NCBI36
NG_012800.1:g.7603C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*45C= MANE Select ENSP00000235382.5:n.*45C=
ENST00000235382.6:c.*45C= ENSP00000235382.5:n.*45C=
NM_002923.3:c.*45C= NP_002914.1:n.*45C=
NM_002923.4:c.*45C= MANE Select NP_002914.1:n.*45C=