Canonical Allele Identifier: CA1401208618
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530534_129530535delinsAC , CM000665.2:g.129530534_129530535delinsAC GRCh38
NC_000003.11:g.129249377_129249378delinsAC , CM000665.1:g.129249377_129249378delinsAC GRCh37
NC_000003.10:g.130732067_130732068delinsAC NCBI36
NG_009115.1:g.6896_6897delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-342_362-341delinsAC MANE Select ENSP00000296271.3:n.362-342_362-341delinsAC
ENST00000296271.3:c.362-342_362-341delinsAC ENSP00000296271.3:n.362-342_362-341delinsAC
NM_000539.3:c.362-342_362-341delinsAC MANE Select NP_000530.1:n.362-342_362-341delinsAC