Canonical Allele Identifier: CA35070412

Gene: RGS2

Linked Data

• dbSNP Id: rs888346499
• gnomAD v2: 1-192781381-A-G
• gnomAD v3: 1-192812251-A-G
• gnomAD v4: 1-192812251-A-G
• MyVariant Identifiers: chr1:g.192781381A>G (hg19) ; chr1:g.192812251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812251A>G , CM000663.2:g.192812251A>G	GRCh38
NC_000001.10:g.192781381A>G , CM000663.1:g.192781381A>G	GRCh37
NC_000001.9:g.191048004A>G	NCBI36
NG_012800.1:g.8213A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*655A>G MANE Select	ENSP00000235382.5:n.*655A>G
ENST00000235382.6:c.*655A>G	ENSP00000235382.5:n.*655A>G
NM_002923.3:c.*655A>G	NP_002914.1:n.*655A>G
NM_002923.4:c.*655A>G MANE Select	NP_002914.1:n.*655A>G