Canonical Allele Identifier: CA2758363936
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531076_129531082del , CM000665.2:g.129531076_129531082del GRCh38
NC_000003.11:g.129249919_129249925del , CM000665.1:g.129249919_129249925del GRCh37
NC_000003.10:g.130732609_130732615del NCBI36
NG_009115.1:g.7438_7444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.530+32_530+38del MANE Select ENSP00000296271.3:n.530+32_530+38del
ENST00000296271.3:c.530+32_530+38del ENSP00000296271.3:n.530+32_530+38del
NM_000539.3:c.530+32_530+38del MANE Select NP_000530.1:n.530+32_530+38del