Canonical Allele Identifier: CA2758361740
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532864_129532865insA , CM000665.2:g.129532864_129532865insA GRCh38
NC_000003.11:g.129251707_129251708insA , CM000665.1:g.129251707_129251708insA GRCh37
NC_000003.10:g.130734397_130734398insA NCBI36
NG_009115.1:g.9226_9227insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+92_936+93insA MANE Select ENSP00000296271.3:n.936+92_936+93insA
ENST00000296271.3:c.936+92_936+93insA ENSP00000296271.3:n.936+92_936+93insA
NM_000539.3:c.936+92_936+93insA MANE Select NP_000530.1:n.936+92_936+93insA