Canonical Allele Identifier: CA35070365

Gene: RGS2

Linked Data

• dbSNP Id: rs868053520
• gnomAD v2: 1-192780966-C-T
• gnomAD v3: 1-192811836-C-T
• gnomAD v4: 1-192811836-C-T
• MyVariant Identifiers: chr1:g.192780966C>T (hg19) ; chr1:g.192811836C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192811836C>T , CM000663.2:g.192811836C>T	GRCh38
NC_000001.10:g.192780966C>T , CM000663.1:g.192780966C>T	GRCh37
NC_000001.9:g.191047589C>T	NCBI36
NG_012800.1:g.7798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*240C>T MANE Select	ENSP00000235382.5:n.*240C>T
ENST00000235382.6:c.*240C>T	ENSP00000235382.5:n.*240C>T
NM_002923.3:c.*240C>T	NP_002914.1:n.*240C>T
NM_002923.4:c.*240C>T MANE Select	NP_002914.1:n.*240C>T