Canonical Allele Identifier: CA359725065
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.193A>C MANE Select ENSP00000282572.4:p.Ser65Arg
ENST00000282572.4:c.193A>C ENSP00000282572.4:p.Ser65Arg
ENST00000501463.2:c.193A>C ENSP00000422485.1:p.Ser65Arg
NM_021147.4:c.193A>C NP_066970.3:p.Ser65Arg
NR_125346.1:n.387A>C
NR_125347.1:n.387A>C
NM_021147.5:c.193A>C MANE Select NP_066970.3:p.Ser65Arg
NR_125346.2:n.278A>C
NR_125347.2:n.278A>C