Canonical Allele Identifier: CA1401205750
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528973_129528976delinsCGTG , CM000665.2:g.129528973_129528976delinsCGTG GRCh38
NC_000003.11:g.129247816_129247819delinsCGTG , CM000665.1:g.129247816_129247819delinsCGTG GRCh37
NC_000003.10:g.130730506_130730509delinsCGTG NCBI36
NG_009115.1:g.5335_5338delinsCGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.240_243delinsCGTG MANE Select ENSP00000296271.3:p.Ala80=
ENST00000296271.3:c.240_243delinsCGTG ENSP00000296271.3:p.Ala80=
NM_000539.3:c.240_243delinsCGTG MANE Select NP_000530.1:p.Ala80=