Canonical Allele Identifier: CA435644296
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1578279796
MyVariant Identifiers: chr3:g.129249886A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531043A>C , CM000665.2:g.129531043A>C GRCh38
NC_000003.11:g.129249886A>C , CM000665.1:g.129249886A>C GRCh37
NC_000003.10:g.130732576A>C NCBI36
NG_009115.1:g.7405A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.529A>C MANE Select ENSP00000296271.3:p.Arg177=
ENST00000296271.3:c.529A>C ENSP00000296271.3:p.Arg177=
NM_000539.3:c.529A>C MANE Select NP_000530.1:p.Arg177=
Search 100 bp 5'
Search 100 bp 3'