Canonical Allele Identifier: CA1215986712
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811653G= , CM000663.2:g.192811653G= GRCh38
NC_000001.10:g.192780783G= , CM000663.1:g.192780783G= GRCh37
NC_000001.9:g.191047406G= NCBI36
NG_012800.1:g.7615G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*57G= MANE Select ENSP00000235382.5:n.*57G=
ENST00000235382.6:c.*57G= ENSP00000235382.5:n.*57G=
NM_002923.3:c.*57G= NP_002914.1:n.*57G=
NM_002923.4:c.*57G= MANE Select NP_002914.1:n.*57G=