Canonical Allele Identifier: CA559800464
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1365106396
gnomAD v2: 5-54528907-A-C
gnomAD v3: 5-55233079-A-C
gnomAD v4: 5-55233079-A-C
MyVariant Identifiers: chr5:g.54528907A>C (hg19) chr5:g.55233079A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233079A>C , CM000667.2:g.55233079A>C GRCh38
NC_000005.9:g.54528907A>C , CM000667.1:g.54528907A>C GRCh37
NC_000005.8:g.54564664A>C NCBI36
NG_034201.1:g.5639T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+64T>G MANE Select ENSP00000282572.4:n.381+64T>G
ENST00000282572.4:c.381+64T>G ENSP00000282572.4:n.381+64T>G
ENST00000501463.2:c.*49T>G ENSP00000422485.1:n.*49T>G
NM_021147.4:c.381+64T>G NP_066970.3:n.381+64T>G
NR_125346.1:n.639T>G
NR_125347.1:n.580+59T>G
NM_021147.5:c.381+64T>G MANE Select NP_066970.3:n.381+64T>G
NR_125346.2:n.530T>G
NR_125347.2:n.471+59T>G
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