Canonical Allele Identifier: CA1547390996
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233609G= , CM000667.2:g.55233609G= GRCh38
NC_000005.9:g.54529437G= , CM000667.1:g.54529437G= GRCh37
NC_000005.8:g.54565194G= NCBI36
NG_034201.1:g.5109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-86C= ENSP00000282572.4:n.-86C=
NM_021147.4:c.-86C= NP_066970.3:n.-86C=
NR_125346.1:n.109C=
NR_125347.1:n.109C=