Canonical Allele Identifier: CA1547391069
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233651T= , CM000667.2:g.55233651T= GRCh38
NC_000005.9:g.54529479T= , CM000667.1:g.54529479T= GRCh37
NC_000005.8:g.54565236T= NCBI36
NG_034201.1:g.5067A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-128A= ENSP00000282572.4:n.-128A=
NM_021147.4:c.-128A= NP_066970.3:n.-128A=
NR_125346.1:n.67A=
NR_125347.1:n.67A=