Canonical Allele Identifier: CA118945653
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1278187
ClinVar RCV Id: RCV001694928
dbSNP Id: rs186617234
gnomAD v2: 5-54529416-C-A
gnomAD v3: 5-55233588-C-A
gnomAD v4: 5-55233588-C-A
MyVariant Identifiers: chr5:g.54529416C>A (hg19) chr5:g.55233588C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233588C>A , CM000667.2:g.55233588C>A GRCh38
NC_000005.9:g.54529416C>A , CM000667.1:g.54529416C>A GRCh37
NC_000005.8:g.54565173C>A NCBI36
NG_034201.1:g.5130G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-65G>T MANE Select ENSP00000282572.4:n.-65G>T
ENST00000282572.4:c.-65G>T ENSP00000282572.4:n.-65G>T
ENST00000501463.2:c.-65G>T ENSP00000422485.1:n.-65G>T
NM_021147.4:c.-65G>T NP_066970.3:n.-65G>T
NR_125346.1:n.130G>T
NR_125347.1:n.130G>T
NM_021147.5:c.-65G>T MANE Select NP_066970.3:n.-65G>T
NR_125346.2:n.21G>T
NR_125347.2:n.21G>T
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