Canonical Allele Identifier: CA1401211656
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532588C= , CM000665.2:g.129532588C= GRCh38
NC_000003.11:g.129251431C= , CM000665.1:g.129251431C= GRCh37
NC_000003.10:g.130734121C= NCBI36
NG_009115.1:g.8950C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.752C= MANE Select ENSP00000296271.3:p.Thr251=
ENST00000296271.3:c.752C= ENSP00000296271.3:p.Thr251=
NM_000539.3:c.752C= MANE Select NP_000530.1:p.Thr251=