Canonical Allele Identifier: CA2758363792
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529226_129529227insA , CM000665.2:g.129529226_129529227insA GRCh38
NC_000003.11:g.129248069_129248070insA , CM000665.1:g.129248069_129248070insA GRCh37
NC_000003.10:g.130730759_130730760insA NCBI36
NG_009115.1:g.5588_5589insA

Transcript Alleles

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