Canonical Allele Identifier: CA35070349
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs11540017
gnomAD v4: 1-192811659-G-T
MyVariant Identifiers: chr1:g.192780789G>T (hg19) chr1:g.192811659G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811659G>T , CM000663.2:g.192811659G>T GRCh38
NC_000001.10:g.192780789G>T , CM000663.1:g.192780789G>T GRCh37
NC_000001.9:g.191047412G>T NCBI36
NG_012800.1:g.7621G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*63G>T MANE Select ENSP00000235382.5:n.*63G>T
ENST00000235382.6:c.*63G>T ENSP00000235382.5:n.*63G>T
NM_002923.3:c.*63G>T NP_002914.1:n.*63G>T
NM_002923.4:c.*63G>T MANE Select NP_002914.1:n.*63G>T
Search 100 bp 5'
Search 100 bp 3'