Canonical Allele Identifier: CA1401205090
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528791G= , CM000665.2:g.129528791G= GRCh38
NC_000003.11:g.129247634G= , CM000665.1:g.129247634G= GRCh37
NC_000003.10:g.130730324G= NCBI36
NG_009115.1:g.5153G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.58G= MANE Select ENSP00000296271.3:p.Val20=
ENST00000296271.3:c.58G= ENSP00000296271.3:p.Val20=
NM_000539.3:c.58G= MANE Select NP_000530.1:p.Val20=