Canonical Allele Identifier: CA1215986708
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811642C= , CM000663.2:g.192811642C= GRCh38
NC_000001.10:g.192780772C= , CM000663.1:g.192780772C= GRCh37
NC_000001.9:g.191047395C= NCBI36
NG_012800.1:g.7604C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*46C= MANE Select ENSP00000235382.5:n.*46C=
ENST00000235382.6:c.*46C= ENSP00000235382.5:n.*46C=
NM_002923.3:c.*46C= NP_002914.1:n.*46C=
NM_002923.4:c.*46C= MANE Select NP_002914.1:n.*46C=