Canonical Allele Identifier: CA898751478
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1553781099

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530533_129530534insCACACACAAC , CM000665.2:g.129530533_129530534insCACACACAAC GRCh38
NC_000003.11:g.129249376_129249377insCACACACAAC , CM000665.1:g.129249376_129249377insCACACACAAC GRCh37
NC_000003.10:g.130732066_130732067insCACACACAAC NCBI36
NG_009115.1:g.6895_6896insCACACACAAC

Transcript Alleles

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