Canonical Allele Identifier: CA898751417
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1553781099
gnomAD v3: 3-129530533-A-ACACACACACAAC
gnomAD v4: 3-129530533-A-ACACACACACAAC
MyVariant Identifiers: chr3:g.129249376_129249377insCACACACACAAC (hg19) chr3:g.129530533_129530534insCACACACACAAC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530533_129530534insCACACACACAAC , CM000665.2:g.129530533_129530534insCACACACACAAC GRCh38
NC_000003.11:g.129249376_129249377insCACACACACAAC , CM000665.1:g.129249376_129249377insCACACACACAAC GRCh37
NC_000003.10:g.130732066_130732067insCACACACACAAC NCBI36
NG_009115.1:g.6895_6896insCACACACACAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-343_362-342insCACACACACAAC MANE Select ENSP00000296271.3:n.362-343_362-342insCACACACACAAC
ENST00000296271.3:c.362-343_362-342insCACACACACAAC ENSP00000296271.3:n.362-343_362-342insCACACACACAAC
NM_000539.3:c.362-343_362-342insCACACACACAAC MANE Select NP_000530.1:n.362-343_362-342insCACACACACAAC
Search 100 bp 5'
Search 100 bp 3'