Canonical Allele Identifier: CA1401204796
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084755166
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528700G>A , CM000665.2:g.129528700G>A GRCh38
NC_000003.11:g.129247543G>A , CM000665.1:g.129247543G>A GRCh37
NC_000003.10:g.130730233G>A NCBI36
NG_009115.1:g.5062G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-34G>A MANE Select ENSP00000296271.3:n.-34G>A
ENST00000296271.3:c.-34G>A ENSP00000296271.3:n.-34G>A
NM_000539.3:c.-34G>A MANE Select NP_000530.1:n.-34G>A
Search 100 bp 5'
Search 100 bp 3'