Canonical Allele Identifier: CA2758361726
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532855del , CM000665.2:g.129532855del GRCh38
NC_000003.11:g.129251698del , CM000665.1:g.129251698del GRCh37
NC_000003.10:g.130734388del NCBI36
NG_009115.1:g.9217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+83del MANE Select ENSP00000296271.3:n.936+83del
ENST00000296271.3:c.936+83del ENSP00000296271.3:n.936+83del
NM_000539.3:c.936+83del MANE Select NP_000530.1:n.936+83del
Search 100 bp 5'
Search 100 bp 3'