Canonical Allele Identifier: CA1215986767
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811813A= , CM000663.2:g.192811813A= GRCh38
NC_000001.10:g.192780943A= , CM000663.1:g.192780943A= GRCh37
NC_000001.9:g.191047566A= NCBI36
NG_012800.1:g.7775A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*217A= MANE Select ENSP00000235382.5:n.*217A=
ENST00000235382.6:c.*217A= ENSP00000235382.5:n.*217A=
NM_002923.3:c.*217A= NP_002914.1:n.*217A=
NM_002923.4:c.*217A= MANE Select NP_002914.1:n.*217A=