Canonical Allele Identifier: CA729320452
Gene: RGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1348156741
gnomAD v3: 1-192811672-G-A
gnomAD v4: 1-192811672-G-A
MyVariant Identifiers: chr1:g.192780802G>A (hg19) chr1:g.192811672G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811672G>A , CM000663.2:g.192811672G>A GRCh38
NC_000001.10:g.192780802G>A , CM000663.1:g.192780802G>A GRCh37
NC_000001.9:g.191047425G>A NCBI36
NG_012800.1:g.7634G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*76G>A MANE Select ENSP00000235382.5:n.*76G>A
ENST00000235382.6:c.*76G>A ENSP00000235382.5:n.*76G>A
NM_002923.3:c.*76G>A NP_002914.1:n.*76G>A
NM_002923.4:c.*76G>A MANE Select NP_002914.1:n.*76G>A
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