Canonical Allele Identifier: CA359725037
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233328A>T , CM000667.2:g.55233328A>T GRCh38
NC_000005.9:g.54529156A>T , CM000667.1:g.54529156A>T GRCh37
NC_000005.8:g.54564913A>T NCBI36
NG_034201.1:g.5390T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.196T>A MANE Select ENSP00000282572.4:p.Ser66Thr
ENST00000282572.4:c.196T>A ENSP00000282572.4:p.Ser66Thr
ENST00000501463.2:c.196T>A ENSP00000422485.1:p.Ser66Thr
NM_021147.4:c.196T>A NP_066970.3:p.Ser66Thr
NR_125346.1:n.390T>A
NR_125347.1:n.390T>A
NM_021147.5:c.196T>A MANE Select NP_066970.3:p.Ser66Thr
NR_125346.2:n.281T>A
NR_125347.2:n.281T>A