Canonical Allele Identifier: CA1215986735
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811722T= , CM000663.2:g.192811722T= GRCh38
NC_000001.10:g.192780852T= , CM000663.1:g.192780852T= GRCh37
NC_000001.9:g.191047475T= NCBI36
NG_012800.1:g.7684T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*126T= MANE Select ENSP00000235382.5:n.*126T=
ENST00000235382.6:c.*126T= ENSP00000235382.5:n.*126T=
NM_002923.3:c.*126T= NP_002914.1:n.*126T=
NM_002923.4:c.*126T= MANE Select NP_002914.1:n.*126T=