Canonical Allele Identifier: CA1401211734
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532602A= , CM000665.2:g.129532602A= GRCh38
NC_000003.11:g.129251445A= , CM000665.1:g.129251445A= GRCh37
NC_000003.10:g.130734135A= NCBI36
NG_009115.1:g.8964A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.766A= MANE Select ENSP00000296271.3:p.Ile256=
ENST00000296271.3:c.766A= ENSP00000296271.3:p.Ile256=
NM_000539.3:c.766A= MANE Select NP_000530.1:p.Ile256=