Canonical Allele Identifier: CA1547391105
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233683C= , CM000667.2:g.55233683C= GRCh38
NC_000005.9:g.54529511C= , CM000667.1:g.54529511C= GRCh37
NC_000005.8:g.54565268C= NCBI36
NG_034201.1:g.5035G=

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-160G= NP_066970.3:n.-160G=
NR_125346.1:n.35G=
NR_125347.1:n.35G=