Canonical Allele Identifier: CA1547391012
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233624C= , CM000667.2:g.55233624C= GRCh38
NC_000005.9:g.54529452C= , CM000667.1:g.54529452C= GRCh37
NC_000005.8:g.54565209C= NCBI36
NG_034201.1:g.5094G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-101G= ENSP00000282572.4:n.-101G=
NM_021147.4:c.-101G= NP_066970.3:n.-101G=
NR_125346.1:n.94G=
NR_125347.1:n.94G=