Canonical Allele Identifier: CA729320491

Gene: RGS2

Linked Data

• dbSNP Id: rs1440011146
• gnomAD v3: 1-192811798-C-G
• gnomAD v4: 1-192811798-C-G
• MyVariant Identifiers: chr1:g.192780928C>G (hg19) ; chr1:g.192811798C>G (hg38)

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