Canonical Allele Identifier: CA2758363803
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529233_129529234del , CM000665.2:g.129529233_129529234del GRCh38
NC_000003.11:g.129248076_129248077del , CM000665.1:g.129248076_129248077del GRCh37
NC_000003.10:g.130730766_130730767del NCBI36
NG_009115.1:g.5595_5596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+139_361+140del MANE Select ENSP00000296271.3:n.361+139_361+140del
ENST00000296271.3:c.361+139_361+140del ENSP00000296271.3:n.361+139_361+140del
NM_000539.3:c.361+139_361+140del MANE Select NP_000530.1:n.361+139_361+140del