Canonical Allele Identifier: CA1401205813
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528980G= , CM000665.2:g.129528980G= GRCh38
NC_000003.11:g.129247823G= , CM000665.1:g.129247823G= GRCh37
NC_000003.10:g.130730513G= NCBI36
NG_009115.1:g.5342G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.247G= MANE Select ENSP00000296271.3:p.Asp83=
ENST00000296271.3:c.247G= ENSP00000296271.3:p.Asp83=
NM_000539.3:c.247G= MANE Select NP_000530.1:p.Asp83=