Canonical Allele Identifier: CA2649611483
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811830T>C , CM000663.2:g.192811830T>C GRCh38
NC_000001.10:g.192780960T>C , CM000663.1:g.192780960T>C GRCh37
NC_000001.9:g.191047583T>C NCBI36
NG_012800.1:g.7792T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*234T>C MANE Select ENSP00000235382.5:n.*234T>C
ENST00000235382.6:c.*234T>C ENSP00000235382.5:n.*234T>C
NM_002923.3:c.*234T>C NP_002914.1:n.*234T>C
NM_002923.4:c.*234T>C MANE Select NP_002914.1:n.*234T>C