Canonical Allele Identifier: CA2667617005
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532417del , CM000665.2:g.129532417del GRCh38
NC_000003.11:g.129251260del , CM000665.1:g.129251260del GRCh37
NC_000003.10:g.130733950del NCBI36
NG_009115.1:g.8779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.696+1del
ENST00000296271.3:c.696+1del
NM_000539.3:c.696+1del