Canonical Allele Identifier: CA2574103251
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811660A>T , CM000663.2:g.192811660A>T GRCh38
NC_000001.10:g.192780790A>T , CM000663.1:g.192780790A>T GRCh37
NC_000001.9:g.191047413A>T NCBI36
NG_012800.1:g.7622A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*64A>T MANE Select ENSP00000235382.5:n.*64A>T
ENST00000235382.6:c.*64A>T ENSP00000235382.5:n.*64A>T
NM_002923.3:c.*64A>T NP_002914.1:n.*64A>T
NM_002923.4:c.*64A>T MANE Select NP_002914.1:n.*64A>T