Canonical Allele Identifier: CA812219182
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1039949642
gnomAD v3: 5-55233687-G-A
gnomAD v4: 5-55233687-G-A
MyVariant Identifiers: chr5:g.54529515G>A (hg19) chr5:g.55233687G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233687G>A , CM000667.2:g.55233687G>A GRCh38
NC_000005.9:g.54529515G>A , CM000667.1:g.54529515G>A GRCh37
NC_000005.8:g.54565272G>A NCBI36
NG_034201.1:g.5031C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-164C>T NP_066970.3:n.-164C>T
NR_125346.1:n.31C>T
NR_125347.1:n.31C>T
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