Canonical Allele Identifier: CA359726388
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 857554
ClinVar RCV Id: RCV001063258 RCV003405280
dbSNP Id: rs1299342018
gnomAD v2: 5-54529336-G-T
gnomAD v3: 5-55233508-G-T
gnomAD v4: 5-55233508-G-T
MyVariant Identifiers: chr5:g.54529336G>T (hg19) chr5:g.55233508G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233508G>T , CM000667.2:g.55233508G>T GRCh38
NC_000005.9:g.54529336G>T , CM000667.1:g.54529336G>T GRCh37
NC_000005.8:g.54565093G>T NCBI36
NG_034201.1:g.5210C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.16C>A MANE Select ENSP00000282572.4:p.Pro6Thr
ENST00000282572.4:c.16C>A ENSP00000282572.4:p.Pro6Thr
ENST00000501463.2:c.16C>A ENSP00000422485.1:p.Pro6Thr
NM_021147.4:c.16C>A NP_066970.3:p.Pro6Thr
NR_125346.1:n.210C>A
NR_125347.1:n.210C>A
NM_021147.5:c.16C>A MANE Select NP_066970.3:p.Pro6Thr
NR_125346.2:n.101C>A
NR_125347.2:n.101C>A
Search 100 bp 5'
Search 100 bp 3'