Canonical Allele Identifier: CA2667616430
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129531033-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531035del , CM000665.2:g.129531035del GRCh38
NC_000003.11:g.129249878del , CM000665.1:g.129249878del GRCh37
NC_000003.10:g.130732568del NCBI36
NG_009115.1:g.7397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.521del MANE Select ENSP00000296271.3:p.Gly174AlafsTer?
ENST00000296271.3:c.521del ENSP00000296271.3:p.Gly174AlafsTer?
NM_000539.3:c.521del MANE Select NP_000530.1:p.Gly174AlafsTer?
Search 100 bp 5'
Search 100 bp 3'