Canonical Allele Identifier: CA35070348
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs141804594
gnomAD v2: 1-192780787-G-A
gnomAD v3: 1-192811657-G-A
gnomAD v4: 1-192811657-G-A
MyVariant Identifiers: chr1:g.192780787G>A (hg19) chr1:g.192811657G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811657G>A , CM000663.2:g.192811657G>A GRCh38
NC_000001.10:g.192780787G>A , CM000663.1:g.192780787G>A GRCh37
NC_000001.9:g.191047410G>A NCBI36
NG_012800.1:g.7619G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*61G>A MANE Select ENSP00000235382.5:n.*61G>A
ENST00000235382.6:c.*61G>A ENSP00000235382.5:n.*61G>A
NM_002923.3:c.*61G>A NP_002914.1:n.*61G>A
NM_002923.4:c.*61G>A MANE Select NP_002914.1:n.*61G>A
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