Canonical Allele Identifier: CA1215986814
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811973T= , CM000663.2:g.192811973T= GRCh38
NC_000001.10:g.192781103T= , CM000663.1:g.192781103T= GRCh37
NC_000001.9:g.191047726T= NCBI36
NG_012800.1:g.7935T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*377T= MANE Select ENSP00000235382.5:n.*377T=
ENST00000235382.6:c.*377T= ENSP00000235382.5:n.*377T=
NM_002923.3:c.*377T= NP_002914.1:n.*377T=
NM_002923.4:c.*377T= MANE Select NP_002914.1:n.*377T=