Canonical Allele Identifier: CA359725115
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1362575
ClinVar RCV Id: RCV001900229
dbSNP Id: rs1745657575
gnomAD v4: 5-55233339-T-C
MyVariant Identifiers: chr5:g.54529167T>C (hg19) chr5:g.55233339T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233339T>C , CM000667.2:g.55233339T>C GRCh38
NC_000005.9:g.54529167T>C , CM000667.1:g.54529167T>C GRCh37
NC_000005.8:g.54564924T>C NCBI36
NG_034201.1:g.5379A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.185A>G MANE Select ENSP00000282572.4:p.Glu62Gly
ENST00000282572.4:c.185A>G ENSP00000282572.4:p.Glu62Gly
ENST00000501463.2:c.185A>G ENSP00000422485.1:p.Glu62Gly
NM_021147.4:c.185A>G NP_066970.3:p.Glu62Gly
NR_125346.1:n.379A>G
NR_125347.1:n.379A>G
NM_021147.5:c.185A>G MANE Select NP_066970.3:p.Glu62Gly
NR_125346.2:n.270A>G
NR_125347.2:n.270A>G
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