Canonical Allele Identifier: CA1547391025
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233632T= , CM000667.2:g.55233632T= GRCh38
NC_000005.9:g.54529460T= , CM000667.1:g.54529460T= GRCh37
NC_000005.8:g.54565217T= NCBI36
NG_034201.1:g.5086A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-109A= ENSP00000282572.4:n.-109A=
NM_021147.4:c.-109A= NP_066970.3:n.-109A=
NR_125346.1:n.86A=
NR_125347.1:n.86A=