Canonical Allele Identifier: CA1401210941
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532268T= , CM000665.2:g.129532268T= GRCh38
NC_000003.11:g.129251111T= , CM000665.1:g.129251111T= GRCh37
NC_000003.10:g.130733801T= NCBI36
NG_009115.1:g.8630T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.548T= MANE Select ENSP00000296271.3:p.Leu183=
ENST00000296271.3:c.548T= ENSP00000296271.3:p.Leu183=
NM_000539.3:c.548T= MANE Select NP_000530.1:p.Leu183=