Canonical Allele Identifier: CA118945684
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1052966401
gnomAD v3: 5-55233610-G-A
gnomAD v4: 5-55233610-G-A
MyVariant Identifiers: chr5:g.54529438G>A (hg19) chr5:g.55233610G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233610G>A , CM000667.2:g.55233610G>A GRCh38
NC_000005.9:g.54529438G>A , CM000667.1:g.54529438G>A GRCh37
NC_000005.8:g.54565195G>A NCBI36
NG_034201.1:g.5108C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-87C>T ENSP00000282572.4:n.-87C>T
NM_021147.4:c.-87C>T NP_066970.3:n.-87C>T
NR_125346.1:n.108C>T
NR_125347.1:n.108C>T
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