Canonical Allele Identifier: CA359726165
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233478-C-A
MyVariant Identifiers: chr5:g.54529306C>A (hg19) chr5:g.55233478C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233478C>A , CM000667.2:g.55233478C>A GRCh38
NC_000005.9:g.54529306C>A , CM000667.1:g.54529306C>A GRCh37
NC_000005.8:g.54565063C>A NCBI36
NG_034201.1:g.5240G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.46G>T MANE Select ENSP00000282572.4:p.Ala16Ser
ENST00000282572.4:c.46G>T ENSP00000282572.4:p.Ala16Ser
ENST00000501463.2:c.46G>T ENSP00000422485.1:p.Ala16Ser
NM_021147.4:c.46G>T NP_066970.3:p.Ala16Ser
NR_125346.1:n.240G>T
NR_125347.1:n.240G>T
NM_021147.5:c.46G>T MANE Select NP_066970.3:p.Ala16Ser
NR_125346.2:n.131G>T
NR_125347.2:n.131G>T
Search 100 bp 5'
Search 100 bp 3'