Canonical Allele Identifier: CA2673856905
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233611_55233623dup , CM000667.2:g.55233611_55233623dup GRCh38
NC_000005.9:g.54529439_54529451dup , CM000667.1:g.54529439_54529451dup GRCh37
NC_000005.8:g.54565196_54565208dup NCBI36
NG_034201.1:g.5097_5109dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-98_-86dup ENSP00000282572.4:n.-98_-86dup
NM_021147.4:c.-98_-86dup NP_066970.3:n.-98_-86dup
NR_125346.1:n.97_109dup
NR_125347.1:n.97_109dup