Canonical Allele Identifier: CA559343766
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1442642887
gnomAD v2: 5-54529479-T-TTC
gnomAD v3: 5-55233651-T-TTC
gnomAD v4: 5-55233651-T-TTC
MyVariant Identifiers: chr5:g.54529479_54529480insTC (hg19) chr5:g.55233651_55233652insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233657_55233658dup , CM000667.2:g.55233657_55233658dup GRCh38
NC_000005.9:g.54529485_54529486dup , CM000667.1:g.54529485_54529486dup GRCh37
NC_000005.8:g.54565242_54565243dup NCBI36
NG_034201.1:g.5065_5066dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-130_-129dup ENSP00000282572.4:n.-130_-129dup
NM_021147.4:c.-130_-129dup NP_066970.3:n.-130_-129dup
NR_125346.1:n.65_66dup
NR_125347.1:n.65_66dup
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