Canonical Allele Identifier: CA729320491
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1440011146

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811798C>G , CM000663.2:g.192811798C>G GRCh38
NC_000001.10:g.192780928C>G , CM000663.1:g.192780928C>G GRCh37
NC_000001.9:g.191047551C>G NCBI36
NG_012800.1:g.7760C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*202C>G MANE Select ENSP00000235382.5:n.*202C>G
ENST00000235382.6:c.*202C>G ENSP00000235382.5:n.*202C>G
NM_002923.3:c.*202C>G NP_002914.1:n.*202C>G
NM_002923.4:c.*202C>G MANE Select NP_002914.1:n.*202C>G