Canonical Allele Identifier: CA1053435656
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1553781099

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530533_129530534insCACAACACACACACAC , CM000665.2:g.129530533_129530534insCACAACACACACACAC GRCh38
NC_000003.11:g.129249376_129249377insCACAACACACACACAC , CM000665.1:g.129249376_129249377insCACAACACACACACAC GRCh37
NC_000003.10:g.130732066_130732067insCACAACACACACACAC NCBI36
NG_009115.1:g.6895_6896insCACAACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-343_362-342insCACAACACACACACAC MANE Select ENSP00000296271.3:n.362-343_362-342insCACAACACACACACAC
ENST00000296271.3:c.362-343_362-342insCACAACACACACACAC ENSP00000296271.3:n.362-343_362-342insCACAACACACACACAC
NM_000539.3:c.362-343_362-342insCACAACACACACACAC MANE Select NP_000530.1:n.362-343_362-342insCACAACACACACACAC