Canonical Allele Identifier: CA1547391013
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233627G= , CM000667.2:g.55233627G= GRCh38
NC_000005.9:g.54529455G= , CM000667.1:g.54529455G= GRCh37
NC_000005.8:g.54565212G= NCBI36
NG_034201.1:g.5091C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-104C= ENSP00000282572.4:n.-104C=
NM_021147.4:c.-104C= NP_066970.3:n.-104C=
NR_125346.1:n.91C=
NR_125347.1:n.91C=