Canonical Allele Identifier: CA1401208199
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530525_129530526delinsAC , CM000665.2:g.129530525_129530526delinsAC GRCh38
NC_000003.11:g.129249368_129249369delinsAC , CM000665.1:g.129249368_129249369delinsAC GRCh37
NC_000003.10:g.130732058_130732059delinsAC NCBI36
NG_009115.1:g.6887_6888delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-351_362-350delinsAC MANE Select ENSP00000296271.3:n.362-351_362-350delinsAC
ENST00000296271.3:c.362-351_362-350delinsAC ENSP00000296271.3:n.362-351_362-350delinsAC
NM_000539.3:c.362-351_362-350delinsAC MANE Select NP_000530.1:n.362-351_362-350delinsAC