Canonical Allele Identifier: CA559343764
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1409694009
gnomAD v2: 5-54529442-C-T
gnomAD v3: 5-55233614-C-T
gnomAD v4: 5-55233614-C-T
MyVariant Identifiers: chr5:g.54529442C>T (hg19) chr5:g.55233614C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233614C>T , CM000667.2:g.55233614C>T GRCh38
NC_000005.9:g.54529442C>T , CM000667.1:g.54529442C>T GRCh37
NC_000005.8:g.54565199C>T NCBI36
NG_034201.1:g.5104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-91G>A ENSP00000282572.4:n.-91G>A
NM_021147.4:c.-91G>A NP_066970.3:n.-91G>A
NR_125346.1:n.104G>A
NR_125347.1:n.104G>A
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