Canonical Allele Identifier: CA898751424
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1553781099
gnomAD v3: 3-129530533-A-ACAACACACACAC
gnomAD v4: 3-129530533-A-ACAACACACACAC
MyVariant Identifiers: chr3:g.129249376_129249377insCAACACACACAC (hg19) chr3:g.129530533_129530534insCAACACACACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530533_129530534insCAACACACACAC , CM000665.2:g.129530533_129530534insCAACACACACAC GRCh38
NC_000003.11:g.129249376_129249377insCAACACACACAC , CM000665.1:g.129249376_129249377insCAACACACACAC GRCh37
NC_000003.10:g.130732066_130732067insCAACACACACAC NCBI36
NG_009115.1:g.6895_6896insCAACACACACAC

Transcript Alleles

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