Canonical Allele Identifier: CA528004659

Gene: RGS2

Linked Data

• dbSNP Id: rs1481230790
• gnomAD v2: 1-192781408-C-CT
• gnomAD v3: 1-192812278-C-CT
• gnomAD v4: 1-192812278-C-CT
• MyVariant Identifiers: chr1:g.192781408_192781409insT (hg19) ; chr1:g.192812278_192812279insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812280dup , CM000663.2:g.192812280dup	GRCh38
NC_000001.10:g.192781410dup , CM000663.1:g.192781410dup	GRCh37
NC_000001.9:g.191048033dup	NCBI36
NG_012800.1:g.8242dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.6:c.*684dup	ENSP00000235382.5:n.*684dup