Canonical Allele Identifier: CA444189568
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs778844840
gnomAD v4: 5-55233470-C-T
MyVariant Identifiers: chr5:g.54529298C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233470C>T , CM000667.2:g.55233470C>T GRCh38
NC_000005.9:g.54529298C>T , CM000667.1:g.54529298C>T GRCh37
NC_000005.8:g.54565055C>T NCBI36
NG_034201.1:g.5248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.54G>A MANE Select ENSP00000282572.4:p.Arg18=
ENST00000282572.4:c.54G>A ENSP00000282572.4:p.Arg18=
ENST00000501463.2:c.54G>A ENSP00000422485.1:p.Arg18=
NM_021147.4:c.54G>A NP_066970.3:p.Arg18=
NR_125346.1:n.248G>A
NR_125347.1:n.248G>A
NM_021147.5:c.54G>A MANE Select NP_066970.3:p.Arg18=
NR_125346.2:n.139G>A
NR_125347.2:n.139G>A
Search 100 bp 5'
Search 100 bp 3'