Canonical Allele Identifier: CA2758361759
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532880del , CM000665.2:g.129532880del GRCh38
NC_000003.11:g.129251723del , CM000665.1:g.129251723del GRCh37
NC_000003.10:g.130734413del NCBI36
NG_009115.1:g.9242del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+108del MANE Select ENSP00000296271.3:n.936+108del
ENST00000296271.3:c.936+108del ENSP00000296271.3:n.936+108del
NM_000539.3:c.936+108del MANE Select NP_000530.1:n.936+108del
Search 100 bp 5'
Search 100 bp 3'