Canonical Allele Identifier: CA435768979
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247783C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528940C>A , CM000665.2:g.129528940C>A GRCh38
NC_000003.11:g.129247783C>A , CM000665.1:g.129247783C>A GRCh37
NC_000003.10:g.130730473C>A NCBI36
NG_009115.1:g.5302C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.207C>A MANE Select ENSP00000296271.3:p.Arg69=
ENST00000296271.3:c.207C>A ENSP00000296271.3:p.Arg69=
NM_000539.3:c.207C>A MANE Select NP_000530.1:p.Arg69=
Search 100 bp 5'
Search 100 bp 3'