Canonical Allele Identifier: CA2758361723
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532841_129532842insAGTA , CM000665.2:g.129532841_129532842insAGTA GRCh38
NC_000003.11:g.129251684_129251685insAGTA , CM000665.1:g.129251684_129251685insAGTA GRCh37
NC_000003.10:g.130734374_130734375insAGTA NCBI36
NG_009115.1:g.9203_9204insAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+69_936+70insAGTA MANE Select ENSP00000296271.3:n.936+69_936+70insAGTA
ENST00000296271.3:c.936+69_936+70insAGTA ENSP00000296271.3:n.936+69_936+70insAGTA
NM_000539.3:c.936+69_936+70insAGTA MANE Select NP_000530.1:n.936+69_936+70insAGTA