Canonical Allele Identifier: CA2758363794
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529226_129529227insAGA , CM000665.2:g.129529226_129529227insAGA GRCh38
NC_000003.11:g.129248069_129248070insAGA , CM000665.1:g.129248069_129248070insAGA GRCh37
NC_000003.10:g.130730759_130730760insAGA NCBI36
NG_009115.1:g.5588_5589insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+132_361+133insAGA MANE Select ENSP00000296271.3:n.361+132_361+133insAGA
ENST00000296271.3:c.361+132_361+133insAGA ENSP00000296271.3:n.361+132_361+133insAGA
NM_000539.3:c.361+132_361+133insAGA MANE Select NP_000530.1:n.361+132_361+133insAGA