Canonical Allele Identifier: CA729320564

Gene: RGS2

Linked Data

• dbSNP Id: rs1215294202
• gnomAD v3: 1-192811904-A-C
• gnomAD v4: 1-192811904-A-C
• MyVariant Identifiers: chr1:g.192781034A>C (hg19) ; chr1:g.192811904A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192811904A>C , CM000663.2:g.192811904A>C	GRCh38
NC_000001.10:g.192781034A>C , CM000663.1:g.192781034A>C	GRCh37
NC_000001.9:g.191047657A>C	NCBI36
NG_012800.1:g.7866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*308A>C MANE Select	ENSP00000235382.5:n.*308A>C
ENST00000235382.6:c.*308A>C	ENSP00000235382.5:n.*308A>C
NM_002923.3:c.*308A>C	NP_002914.1:n.*308A>C
NM_002923.4:c.*308A>C MANE Select	NP_002914.1:n.*308A>C