Canonical Allele Identifier: CA118945748
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs937187132
gnomAD v3: 5-55233631-C-T
gnomAD v4: 5-55233631-C-T
MyVariant Identifiers: chr5:g.54529459C>T (hg19) chr5:g.55233631C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233631C>T , CM000667.2:g.55233631C>T GRCh38
NC_000005.9:g.54529459C>T , CM000667.1:g.54529459C>T GRCh37
NC_000005.8:g.54565216C>T NCBI36
NG_034201.1:g.5087G>A

Transcript Alleles

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