Canonical Allele Identifier: CA2838624582
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532461_129532465del , CM000665.2:g.129532461_129532465del GRCh38
NC_000003.11:g.129251304_129251308del , CM000665.1:g.129251304_129251308del GRCh37
NC_000003.10:g.130733994_130733998del NCBI36
NG_009115.1:g.8823_8827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.696+45_696+49del MANE Select ENSP00000296271.3:n.696+45_696+49del
ENST00000296271.3:c.696+45_696+49del ENSP00000296271.3:n.696+45_696+49del
NM_000539.3:c.696+45_696+49del MANE Select NP_000530.1:n.696+45_696+49del