Canonical Allele Identifier: CA2673856298
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs2111720468
gnomAD v4: 5-55232925-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232925T>C , CM000667.2:g.55232925T>C GRCh38
NC_000005.9:g.54528753T>C , CM000667.1:g.54528753T>C GRCh37
NC_000005.8:g.54564510T>C NCBI36
NG_034201.1:g.5793A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+218A>G MANE Select ENSP00000282572.4:n.381+218A>G
ENST00000282572.4:c.381+218A>G ENSP00000282572.4:n.381+218A>G
ENST00000501463.2:c.*203A>G ENSP00000422485.1:n.*203A>G
NM_021147.4:c.381+218A>G NP_066970.3:n.381+218A>G
NR_125346.1:n.793A>G
NR_125347.1:n.580+213A>G
NR_125348.1:n.67A>G
NM_021147.5:c.381+218A>G MANE Select NP_066970.3:n.381+218A>G
NR_125346.2:n.684A>G
NR_125347.2:n.471+213A>G
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