Canonical Allele Identifier: CA2543034355
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530830C>A , CM000665.2:g.129530830C>A GRCh38
NC_000003.11:g.129249673C>A , CM000665.1:g.129249673C>A GRCh37
NC_000003.10:g.130732363C>A NCBI36
NG_009115.1:g.7192C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-46C>A MANE Select ENSP00000296271.3:n.362-46C>A
ENST00000296271.3:c.362-46C>A ENSP00000296271.3:n.362-46C>A
NM_000539.3:c.362-46C>A MANE Select NP_000530.1:n.362-46C>A