Canonical Allele Identifier: CA2577961804
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532528T>A , CM000665.2:g.129532528T>A GRCh38
NC_000003.11:g.129251371T>A , CM000665.1:g.129251371T>A GRCh37
NC_000003.10:g.130734061T>A NCBI36
NG_009115.1:g.8890T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.697-5T>A MANE Select ENSP00000296271.3:n.697-5T>A
ENST00000296271.3:c.697-5T>A ENSP00000296271.3:n.697-5T>A
NM_000539.3:c.697-5T>A MANE Select NP_000530.1:n.697-5T>A