Canonical Allele Identifier: CA35070359
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs767891880
MyVariant Identifiers: chr1:g.192780929T>G (hg19) chr1:g.192811799T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811799T>G , CM000663.2:g.192811799T>G GRCh38
NC_000001.10:g.192780929T>G , CM000663.1:g.192780929T>G GRCh37
NC_000001.9:g.191047552T>G NCBI36
NG_012800.1:g.7761T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*203T>G MANE Select ENSP00000235382.5:n.*203T>G
ENST00000235382.6:c.*203T>G ENSP00000235382.5:n.*203T>G
NM_002923.3:c.*203T>G NP_002914.1:n.*203T>G
NM_002923.4:c.*203T>G MANE Select NP_002914.1:n.*203T>G
Search 100 bp 5'
Search 100 bp 3'