Canonical Allele Identifier: CA2607354
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1406832
ClinVar RCV Id: RCV001907005
dbSNP Id: rs200095648
ExAC: 3:129252505 G / A
gnomAD v2: 3-129252505-G-A
gnomAD v3: 3-129533662-G-A
gnomAD v4: 3-129533662-G-A
MyVariant Identifiers: chr3:g.129252505G>A (hg19) chr3:g.129533662G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533662G>A , CM000665.2:g.129533662G>A GRCh38
NC_000003.11:g.129252505G>A , CM000665.1:g.129252505G>A GRCh37
NC_000003.10:g.130735195G>A NCBI36
NG_009115.1:g.10024G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.991G>A MANE Select ENSP00000296271.3:p.Asp331Asn
ENST00000296271.3:c.991G>A ENSP00000296271.3:p.Asp331Asn
NM_000539.3:c.991G>A MANE Select NP_000530.1:p.Asp331Asn
Search 100 bp 5'
Search 100 bp 3'