Canonical Allele Identifier: CA3266808

Gene: CCNO

Linked Data

• ClinVar Variation Id: 697047
• ClinVar RCV Id: RCV001440268
• dbSNP Id: rs191035273
• ExAC: 5:54529019 C / T
• gnomAD v2: 5-54529019-C-T
• gnomAD v3: 5-55233191-C-T
• gnomAD v4: 5-55233191-C-T
• MyVariant Identifiers: chr5:g.54529019C>T (hg19) ; chr5:g.55233191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233191C>T , CM000667.2:g.55233191C>T	GRCh38
NC_000005.9:g.54529019C>T , CM000667.1:g.54529019C>T	GRCh37
NC_000005.8:g.54564776C>T	NCBI36
NG_034201.1:g.5527G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.333G>A MANE Select	ENSP00000282572.4:p.Ala111=
ENST00000282572.4:c.333G>A	ENSP00000282572.4:p.Ala111=
ENST00000501463.2:c.333G>A	ENSP00000422485.1:p.Ala111=
NM_021147.4:c.333G>A	NP_066970.3:p.Ala111=
NR_125346.1:n.527G>A
NR_125347.1:n.527G>A
NM_021147.5:c.333G>A MANE Select	NP_066970.3:p.Ala111=
NR_125346.2:n.418G>A
NR_125347.2:n.418G>A