Canonical Allele Identifier: CA2673856924
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233627_55233649dup , CM000667.2:g.55233627_55233649dup GRCh38
NC_000005.9:g.54529455_54529477dup , CM000667.1:g.54529455_54529477dup GRCh37
NC_000005.8:g.54565212_54565234dup NCBI36
NG_034201.1:g.5070_5092dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-125_-103dup ENSP00000282572.4:n.-125_-103dup
NM_021147.4:c.-125_-103dup NP_066970.3:n.-125_-103dup
NR_125346.1:n.70_92dup
NR_125347.1:n.70_92dup