Canonical Allele Identifier: CA359721325
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55231691-T-C
MyVariant Identifiers: chr5:g.54527519T>C (hg19) chr5:g.55231691T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231691T>C , CM000667.2:g.55231691T>C GRCh38
NC_000005.9:g.54527519T>C , CM000667.1:g.54527519T>C GRCh37
NC_000005.8:g.54563276T>C NCBI36
NG_034201.1:g.7027A>G
NG_051620.1:g.625A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.737A>G MANE Select ENSP00000282572.4:p.Glu246Gly
ENST00000282572.4:c.737A>G ENSP00000282572.4:p.Glu246Gly
ENST00000501463.2:c.*717A>G ENSP00000422485.1:n.*717A>G
NM_021147.4:c.737A>G NP_066970.3:p.Glu246Gly
NR_125346.1:n.1307A>G
NR_125347.1:n.936A>G
NR_125348.1:n.801A>G
NM_021147.5:c.737A>G MANE Select NP_066970.3:p.Glu246Gly
NR_125346.2:n.1198A>G
NR_125347.2:n.827A>G
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