Canonical Allele Identifier: CA2673856938
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233636del , CM000667.2:g.55233636del GRCh38
NC_000005.9:g.54529464del , CM000667.1:g.54529464del GRCh37
NC_000005.8:g.54565221del NCBI36
NG_034201.1:g.5082del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-113del ENSP00000282572.4:n.-113del
NM_021147.4:c.-113del NP_066970.3:n.-113del
NR_125346.1:n.82del
NR_125347.1:n.82del