Canonical Allele Identifier: CA359726203
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233489G>T , CM000667.2:g.55233489G>T GRCh38
NC_000005.9:g.54529317G>T , CM000667.1:g.54529317G>T GRCh37
NC_000005.8:g.54565074G>T NCBI36
NG_034201.1:g.5229C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.35C>A MANE Select ENSP00000282572.4:p.Pro12His
ENST00000282572.4:c.35C>A ENSP00000282572.4:p.Pro12His
ENST00000501463.2:c.35C>A ENSP00000422485.1:p.Pro12His
NM_021147.4:c.35C>A NP_066970.3:p.Pro12His
NR_125346.1:n.229C>A
NR_125347.1:n.229C>A
NM_021147.5:c.35C>A MANE Select NP_066970.3:p.Pro12His
NR_125346.2:n.120C>A
NR_125347.2:n.120C>A