Canonical Allele Identifier: CA359724963
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 846075
ClinVar RCV Id: RCV001049282
dbSNP Id: rs369830529
gnomAD v2: 5-54529144-C-T
gnomAD v3: 5-55233316-C-T
gnomAD v4: 5-55233316-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233316C>T , CM000667.2:g.55233316C>T GRCh38
NC_000005.9:g.54529144C>T , CM000667.1:g.54529144C>T GRCh37
NC_000005.8:g.54564901C>T NCBI36
NG_034201.1:g.5402G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.208G>A MANE Select ENSP00000282572.4:p.Gly70Ser
ENST00000282572.4:c.208G>A ENSP00000282572.4:p.Gly70Ser
ENST00000501463.2:c.208G>A ENSP00000422485.1:p.Gly70Ser
NM_021147.4:c.208G>A NP_066970.3:p.Gly70Ser
NR_125346.1:n.402G>A
NR_125347.1:n.402G>A
NM_021147.5:c.208G>A MANE Select NP_066970.3:p.Gly70Ser
NR_125346.2:n.293G>A
NR_125347.2:n.293G>A