Canonical Allele Identifier: CA359721309
Gene: CCNO HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.54527513C>T (hg19) chr5:g.55231685C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231685C>T , CM000667.2:g.55231685C>T GRCh38
NC_000005.9:g.54527513C>T , CM000667.1:g.54527513C>T GRCh37
NC_000005.8:g.54563270C>T NCBI36
NG_034201.1:g.7033G>A
NG_051620.1:g.631G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.743G>A MANE Select ENSP00000282572.4:p.Gly248Glu
ENST00000282572.4:c.743G>A ENSP00000282572.4:p.Gly248Glu
ENST00000501463.2:c.*723G>A ENSP00000422485.1:n.*723G>A
NM_021147.4:c.743G>A NP_066970.3:p.Gly248Glu
NR_125346.1:n.1313G>A
NR_125347.1:n.942G>A
NR_125348.1:n.807G>A
NM_021147.5:c.743G>A MANE Select NP_066970.3:p.Gly248Glu
NR_125346.2:n.1204G>A
NR_125347.2:n.833G>A
Search 100 bp 5'
Search 100 bp 3'