Canonical Allele Identifier: CA559343767
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1374394885
gnomAD v2: 5-54529518-C-T
gnomAD v3: 5-55233690-C-T
gnomAD v4: 5-55233690-C-T
MyVariant Identifiers: chr5:g.54529518C>T (hg19) chr5:g.55233690C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233690C>T , CM000667.2:g.55233690C>T GRCh38
NC_000005.9:g.54529518C>T , CM000667.1:g.54529518C>T GRCh37
NC_000005.8:g.54565275C>T NCBI36
NG_034201.1:g.5028G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-167G>A NP_066970.3:n.-167G>A
NR_125346.1:n.28G>A
NR_125347.1:n.28G>A
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