Canonical Allele Identifier: CA729320582

Gene: RGS2

Linked Data

• dbSNP Id: rs1464855771
• gnomAD v3: 1-192811951-T-C
• gnomAD v4: 1-192811951-T-C
• MyVariant Identifiers: chr1:g.192781081T>C (hg19) ; chr1:g.192811951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192811951T>C , CM000663.2:g.192811951T>C	GRCh38
NC_000001.10:g.192781081T>C , CM000663.1:g.192781081T>C	GRCh37
NC_000001.9:g.191047704T>C	NCBI36
NG_012800.1:g.7913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*355T>C MANE Select	ENSP00000235382.5:n.*355T>C
ENST00000235382.6:c.*355T>C	ENSP00000235382.5:n.*355T>C
NM_002923.3:c.*355T>C	NP_002914.1:n.*355T>C
NM_002923.4:c.*355T>C MANE Select	NP_002914.1:n.*355T>C