Canonical Allele Identifier: CA1401205688
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528953T= , CM000665.2:g.129528953T= GRCh38
NC_000003.11:g.129247796T= , CM000665.1:g.129247796T= GRCh37
NC_000003.10:g.130730486T= NCBI36
NG_009115.1:g.5315T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.220T= MANE Select ENSP00000296271.3:p.Tyr74=
ENST00000296271.3:c.220T= ENSP00000296271.3:p.Tyr74=
NM_000539.3:c.220T= MANE Select NP_000530.1:p.Tyr74=