Canonical Allele Identifier: CA1215986719
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811672G= , CM000663.2:g.192811672G= GRCh38
NC_000001.10:g.192780802G= , CM000663.1:g.192780802G= GRCh37
NC_000001.9:g.191047425G= NCBI36
NG_012800.1:g.7634G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*76G= MANE Select ENSP00000235382.5:n.*76G=
ENST00000235382.6:c.*76G= ENSP00000235382.5:n.*76G=
NM_002923.3:c.*76G= NP_002914.1:n.*76G=
NM_002923.4:c.*76G= MANE Select NP_002914.1:n.*76G=