Canonical Allele Identifier: CA2667615949
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129529242-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529245del , CM000665.2:g.129529245del GRCh38
NC_000003.11:g.129248088del , CM000665.1:g.129248088del GRCh37
NC_000003.10:g.130730778del NCBI36
NG_009115.1:g.5607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+151del MANE Select ENSP00000296271.3:n.361+151del
ENST00000296271.3:c.361+151del ENSP00000296271.3:n.361+151del
NM_000539.3:c.361+151del MANE Select NP_000530.1:n.361+151del
Search 100 bp 5'
Search 100 bp 3'