Canonical Allele Identifier: CA359721119
Gene: CCNO HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.54527459G>C (hg19) chr5:g.55231631G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231631G>C , CM000667.2:g.55231631G>C GRCh38
NC_000005.9:g.54527459G>C , CM000667.1:g.54527459G>C GRCh37
NC_000005.8:g.54563216G>C NCBI36
NG_034201.1:g.7087C>G
NG_051620.1:g.685C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.797C>G MANE Select ENSP00000282572.4:p.Ala266Gly
ENST00000282572.4:c.797C>G ENSP00000282572.4:p.Ala266Gly
ENST00000501463.2:c.*777C>G ENSP00000422485.1:n.*777C>G
NM_021147.4:c.797C>G NP_066970.3:p.Ala266Gly
NR_125346.1:n.1367C>G
NR_125347.1:n.996C>G
NR_125348.1:n.861C>G
NM_021147.5:c.797C>G MANE Select NP_066970.3:p.Ala266Gly
NR_125346.2:n.1258C>G
NR_125347.2:n.887C>G
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