Canonical Allele Identifier: CA354499146
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1038982
ClinVar RCV Id: RCV001342371
dbSNP Id: rs2084785574
MyVariant Identifiers: chr3:g.129251108G>A (hg19) chr3:g.129532265G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532265G>A , CM000665.2:g.129532265G>A GRCh38
NC_000003.11:g.129251108G>A , CM000665.1:g.129251108G>A GRCh37
NC_000003.10:g.130733798G>A NCBI36
NG_009115.1:g.8627G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.545G>A MANE Select ENSP00000296271.3:p.Gly182Asp
ENST00000296271.3:c.545G>A ENSP00000296271.3:p.Gly182Asp
NM_000539.3:c.545G>A MANE Select NP_000530.1:p.Gly182Asp
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