Canonical Allele Identifier: CA2747137515
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811797A>C , CM000663.2:g.192811797A>C GRCh38
NC_000001.10:g.192780927A>C , CM000663.1:g.192780927A>C GRCh37
NC_000001.9:g.191047550A>C NCBI36
NG_012800.1:g.7759A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*201A>C MANE Select ENSP00000235382.5:n.*201A>C
ENST00000235382.6:c.*201A>C ENSP00000235382.5:n.*201A>C
NM_002923.3:c.*201A>C NP_002914.1:n.*201A>C
NM_002923.4:c.*201A>C MANE Select NP_002914.1:n.*201A>C