Canonical Allele Identifier: CA2607154
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1503722
ClinVar RCV Id: RCV002025656
dbSNP Id: rs778626065
ExAC: 3:129249766 G / A
gnomAD v2: 3-129249766-G-A
gnomAD v3: 3-129530923-G-A
gnomAD v4: 3-129530923-G-A
COSMIC: COSM3060233
MyVariant Identifiers: chr3:g.129249766G>A (hg19) chr3:g.129530923G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530923G>A , CM000665.2:g.129530923G>A GRCh38
NC_000003.11:g.129249766G>A , CM000665.1:g.129249766G>A GRCh37
NC_000003.10:g.130732456G>A NCBI36
NG_009115.1:g.7285G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.409G>A MANE Select ENSP00000296271.3:p.Val137Met
ENST00000296271.3:c.409G>A ENSP00000296271.3:p.Val137Met
NM_000539.3:c.409G>A MANE Select NP_000530.1:p.Val137Met
Search 100 bp 5'
Search 100 bp 3'