Canonical Allele Identifier: CA812219159
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1364908109
gnomAD v3: 5-55233640-CG-C
gnomAD v4: 5-55233640-CG-C
MyVariant Identifiers: chr5:g.54529469del (hg19) chr5:g.55233641del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233642del , CM000667.2:g.55233642del GRCh38
NC_000005.9:g.54529470del , CM000667.1:g.54529470del GRCh37
NC_000005.8:g.54565227del NCBI36
NG_034201.1:g.5077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-118del ENSP00000282572.4:n.-118del
NM_021147.4:c.-118del NP_066970.3:n.-118del
NR_125346.1:n.77del
NR_125347.1:n.77del
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