Canonical Allele Identifier: CA359725457
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233385T>C , CM000667.2:g.55233385T>C GRCh38
NC_000005.9:g.54529213T>C , CM000667.1:g.54529213T>C GRCh37
NC_000005.8:g.54564970T>C NCBI36
NG_034201.1:g.5333A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.139A>G MANE Select ENSP00000282572.4:p.Asn47Asp
ENST00000282572.4:c.139A>G ENSP00000282572.4:p.Asn47Asp
ENST00000501463.2:c.139A>G ENSP00000422485.1:p.Asn47Asp
NM_021147.4:c.139A>G NP_066970.3:p.Asn47Asp
NR_125346.1:n.333A>G
NR_125347.1:n.333A>G
NM_021147.5:c.139A>G MANE Select NP_066970.3:p.Asn47Asp
NR_125346.2:n.224A>G
NR_125347.2:n.224A>G