Canonical Allele Identifier: CA2758361741
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532867del , CM000665.2:g.129532867del GRCh38
NC_000003.11:g.129251710del , CM000665.1:g.129251710del GRCh37
NC_000003.10:g.130734400del NCBI36
NG_009115.1:g.9229del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+95del MANE Select ENSP00000296271.3:n.936+95del
ENST00000296271.3:c.936+95del ENSP00000296271.3:n.936+95del
NM_000539.3:c.936+95del MANE Select NP_000530.1:n.936+95del
Search 100 bp 5'
Search 100 bp 3'