Canonical Allele Identifier: CA648379649
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528683_129528684insA , CM000665.2:g.129528683_129528684insA GRCh38
NC_000003.11:g.129247526_129247527insA , CM000665.1:g.129247526_129247527insA GRCh37
NC_000003.10:g.130730216_130730217insA NCBI36
NG_009115.1:g.5045_5046insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-51_-50insA MANE Select ENSP00000296271.3:n.-51_-50insA
ENST00000296271.3:c.-51_-50insA ENSP00000296271.3:n.-51_-50insA
NM_000539.3:c.-51_-50insA MANE Select NP_000530.1:n.-51_-50insA