Canonical Allele Identifier: CA2500337295
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233615dup , CM000667.2:g.55233615dup GRCh38
NC_000005.9:g.54529443dup , CM000667.1:g.54529443dup GRCh37
NC_000005.8:g.54565200dup NCBI36
NG_034201.1:g.5103dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-92dup ENSP00000282572.4:n.-92dup
NM_021147.4:c.-92dup NP_066970.3:n.-92dup
NR_125346.1:n.103dup
NR_125347.1:n.103dup