Canonical Allele Identifier: CA359725059
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745656857
gnomAD v3: 5-55233331-T-A
gnomAD v4: 5-55233331-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233331T>A , CM000667.2:g.55233331T>A GRCh38
NC_000005.9:g.54529159T>A , CM000667.1:g.54529159T>A GRCh37
NC_000005.8:g.54564916T>A NCBI36
NG_034201.1:g.5387A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.193A>T MANE Select ENSP00000282572.4:p.Ser65Cys
ENST00000282572.4:c.193A>T ENSP00000282572.4:p.Ser65Cys
ENST00000501463.2:c.193A>T ENSP00000422485.1:p.Ser65Cys
NM_021147.4:c.193A>T NP_066970.3:p.Ser65Cys
NR_125346.1:n.387A>T
NR_125347.1:n.387A>T
NM_021147.5:c.193A>T MANE Select NP_066970.3:p.Ser65Cys
NR_125346.2:n.278A>T
NR_125347.2:n.278A>T