Canonical Allele Identifier: CA1547391027
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233633A= , CM000667.2:g.55233633A= GRCh38
NC_000005.9:g.54529461A= , CM000667.1:g.54529461A= GRCh37
NC_000005.8:g.54565218A= NCBI36
NG_034201.1:g.5085T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-110T= ENSP00000282572.4:n.-110T=
NM_021147.4:c.-110T= NP_066970.3:n.-110T=
NR_125346.1:n.85T=
NR_125347.1:n.85T=