Canonical Allele Identifier: CA1547391002
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233612C= , CM000667.2:g.55233612C= GRCh38
NC_000005.9:g.54529440C= , CM000667.1:g.54529440C= GRCh37
NC_000005.8:g.54565197C= NCBI36
NG_034201.1:g.5106G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-89G= ENSP00000282572.4:n.-89G=
NM_021147.4:c.-89G= NP_066970.3:n.-89G=
NR_125346.1:n.106G=
NR_125347.1:n.106G=