Canonical Allele Identifier: CA528004642

Gene: RGS2

Linked Data

• dbSNP Id: rs955383362
• gnomAD v2: 1-192780948-G-T
• gnomAD v3: 1-192811818-G-T
• gnomAD v4: 1-192811818-G-T
• MyVariant Identifiers: chr1:g.192780948G>T (hg19) ; chr1:g.192811818G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192811818G>T , CM000663.2:g.192811818G>T	GRCh38
NC_000001.10:g.192780948G>T , CM000663.1:g.192780948G>T	GRCh37
NC_000001.9:g.191047571G>T	NCBI36
NG_012800.1:g.7780G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*222G>T MANE Select	ENSP00000235382.5:n.*222G>T
ENST00000235382.6:c.*222G>T	ENSP00000235382.5:n.*222G>T
NM_002923.3:c.*222G>T	NP_002914.1:n.*222G>T
NM_002923.4:c.*222G>T MANE Select	NP_002914.1:n.*222G>T