Canonical Allele Identifier: CA118945807
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1023801197
gnomAD v4: 5-55233673-C-A
MyVariant Identifiers: chr5:g.54529501C>A (hg19) chr5:g.55233673C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233673C>A , CM000667.2:g.55233673C>A GRCh38
NC_000005.9:g.54529501C>A , CM000667.1:g.54529501C>A GRCh37
NC_000005.8:g.54565258C>A NCBI36
NG_034201.1:g.5045G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-150G>T ENSP00000282572.4:n.-150G>T
NM_021147.4:c.-150G>T NP_066970.3:n.-150G>T
NR_125346.1:n.45G>T
NR_125347.1:n.45G>T
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