Canonical Allele Identifier: CA1547391009
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233621T= , CM000667.2:g.55233621T= GRCh38
NC_000005.9:g.54529449T= , CM000667.1:g.54529449T= GRCh37
NC_000005.8:g.54565206T= NCBI36
NG_034201.1:g.5097A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-98A= ENSP00000282572.4:n.-98A=
NM_021147.4:c.-98A= NP_066970.3:n.-98A=
NR_125346.1:n.97A=
NR_125347.1:n.97A=