Canonical Allele Identifier: CA1547391092
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233668C= , CM000667.2:g.55233668C= GRCh38
NC_000005.9:g.54529496C= , CM000667.1:g.54529496C= GRCh37
NC_000005.8:g.54565253C= NCBI36
NG_034201.1:g.5050G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-145G= ENSP00000282572.4:n.-145G=
NM_021147.4:c.-145G= NP_066970.3:n.-145G=
NR_125346.1:n.50G=
NR_125347.1:n.50G=