Canonical Allele Identifier: CA2673856539
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233123-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233123T>C , CM000667.2:g.55233123T>C GRCh38
NC_000005.9:g.54528951T>C , CM000667.1:g.54528951T>C GRCh37
NC_000005.8:g.54564708T>C NCBI36
NG_034201.1:g.5595A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+20A>G MANE Select ENSP00000282572.4:n.381+20A>G
ENST00000282572.4:c.381+20A>G ENSP00000282572.4:n.381+20A>G
ENST00000501463.2:c.*5A>G ENSP00000422485.1:n.*5A>G
NM_021147.4:c.381+20A>G NP_066970.3:n.381+20A>G
NR_125346.1:n.595A>G
NR_125347.1:n.580+15A>G
NM_021147.5:c.381+20A>G MANE Select NP_066970.3:n.381+20A>G
NR_125346.2:n.486A>G
NR_125347.2:n.471+15A>G
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