Canonical Allele Identifier: CA648379651
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528691_129528692insA , CM000665.2:g.129528691_129528692insA GRCh38
NC_000003.11:g.129247534_129247535insA , CM000665.1:g.129247534_129247535insA GRCh37
NC_000003.10:g.130730224_130730225insA NCBI36
NG_009115.1:g.5053_5054insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-43_-42insA MANE Select ENSP00000296271.3:n.-43_-42insA
ENST00000296271.3:c.-43_-42insA ENSP00000296271.3:n.-43_-42insA
NM_000539.3:c.-43_-42insA MANE Select NP_000530.1:n.-43_-42insA