Canonical Allele Identifier: CA2667616700
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532227-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532227G>A , CM000665.2:g.129532227G>A GRCh38
NC_000003.11:g.129251070G>A , CM000665.1:g.129251070G>A GRCh37
NC_000003.10:g.130733760G>A NCBI36
NG_009115.1:g.8589G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-24G>A MANE Select ENSP00000296271.3:n.531-24G>A
ENST00000296271.3:c.531-24G>A ENSP00000296271.3:n.531-24G>A
NM_000539.3:c.531-24G>A MANE Select NP_000530.1:n.531-24G>A
Search 100 bp 5'
Search 100 bp 3'