Canonical Allele Identifier: CA1547391006
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233619G= , CM000667.2:g.55233619G= GRCh38
NC_000005.9:g.54529447G= , CM000667.1:g.54529447G= GRCh37
NC_000005.8:g.54565204G= NCBI36
NG_034201.1:g.5099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-96C= ENSP00000282572.4:n.-96C=
NM_021147.4:c.-96C= NP_066970.3:n.-96C=
NR_125346.1:n.99C=
NR_125347.1:n.99C=