Canonical Allele Identifier: CA118945806
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1012469785
gnomAD v3: 5-55233672-C-A
gnomAD v4: 5-55233672-C-A
MyVariant Identifiers: chr5:g.54529500C>A (hg19) chr5:g.55233672C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233672C>A , CM000667.2:g.55233672C>A GRCh38
NC_000005.9:g.54529500C>A , CM000667.1:g.54529500C>A GRCh37
NC_000005.8:g.54565257C>A NCBI36
NG_034201.1:g.5046G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-149G>T ENSP00000282572.4:n.-149G>T
NM_021147.4:c.-149G>T NP_066970.3:n.-149G>T
NR_125346.1:n.46G>T
NR_125347.1:n.46G>T
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