Canonical Allele Identifier: CA2758363777
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529220_129529221insC , CM000665.2:g.129529220_129529221insC GRCh38
NC_000003.11:g.129248063_129248064insC , CM000665.1:g.129248063_129248064insC GRCh37
NC_000003.10:g.130730753_130730754insC NCBI36
NG_009115.1:g.5582_5583insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+126_361+127insC MANE Select ENSP00000296271.3:n.361+126_361+127insC
ENST00000296271.3:c.361+126_361+127insC ENSP00000296271.3:n.361+126_361+127insC
NM_000539.3:c.361+126_361+127insC MANE Select NP_000530.1:n.361+126_361+127insC