Canonical Allele Identifier: CA435769034
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1338813260
MyVariant Identifiers: chr3:g.129251378C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532535C>A , CM000665.2:g.129532535C>A GRCh38
NC_000003.11:g.129251378C>A , CM000665.1:g.129251378C>A GRCh37
NC_000003.10:g.130734068C>A NCBI36
NG_009115.1:g.8897C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.699C>A MANE Select ENSP00000296271.3:p.Ala233=
ENST00000296271.3:c.699C>A ENSP00000296271.3:p.Ala233=
NM_000539.3:c.699C>A MANE Select NP_000530.1:p.Ala233=
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