Canonical Allele Identifier: CA2758363784
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529224_129529229del , CM000665.2:g.129529224_129529229del GRCh38
NC_000003.11:g.129248067_129248072del , CM000665.1:g.129248067_129248072del GRCh37
NC_000003.10:g.130730757_130730762del NCBI36
NG_009115.1:g.5586_5591del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+130_361+135del MANE Select ENSP00000296271.3:n.361+130_361+135del
ENST00000296271.3:c.361+130_361+135del ENSP00000296271.3:n.361+130_361+135del
NM_000539.3:c.361+130_361+135del MANE Select NP_000530.1:n.361+130_361+135del