Canonical Allele Identifier: CA1401208825
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530538_129530539delinsAC , CM000665.2:g.129530538_129530539delinsAC GRCh38
NC_000003.11:g.129249381_129249382delinsAC , CM000665.1:g.129249381_129249382delinsAC GRCh37
NC_000003.10:g.130732071_130732072delinsAC NCBI36
NG_009115.1:g.6900_6901delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-338_362-337delinsAC MANE Select ENSP00000296271.3:n.362-338_362-337delinsAC
ENST00000296271.3:c.362-338_362-337delinsAC ENSP00000296271.3:n.362-338_362-337delinsAC
NM_000539.3:c.362-338_362-337delinsAC MANE Select NP_000530.1:n.362-338_362-337delinsAC