Canonical Allele Identifier: CA1547391032
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233635G= , CM000667.2:g.55233635G= GRCh38
NC_000005.9:g.54529463G= , CM000667.1:g.54529463G= GRCh37
NC_000005.8:g.54565220G= NCBI36
NG_034201.1:g.5083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-112C= ENSP00000282572.4:n.-112C=
NM_021147.4:c.-112C= NP_066970.3:n.-112C=
NR_125346.1:n.83C=
NR_125347.1:n.83C=