Canonical Allele Identifier: CA2607873342

Gene: CCNO

Linked Data

• dbSNP Id: rs2111720806
• gnomAD v4: 5-55233032-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233032A>C , CM000667.2:g.55233032A>C	GRCh38
NC_000005.9:g.54528860A>C , CM000667.1:g.54528860A>C	GRCh37
NC_000005.8:g.54564617A>C	NCBI36
NG_034201.1:g.5686T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+111T>G MANE Select	ENSP00000282572.4:n.381+111T>G
ENST00000282572.4:c.381+111T>G	ENSP00000282572.4:n.381+111T>G
ENST00000501463.2:c.*96T>G	ENSP00000422485.1:n.*96T>G
NM_021147.4:c.381+111T>G	NP_066970.3:n.381+111T>G
NR_125346.1:n.686T>G
NR_125347.1:n.580+106T>G
NM_021147.5:c.381+111T>G MANE Select	NP_066970.3:n.381+111T>G
NR_125346.2:n.577T>G
NR_125347.2:n.471+106T>G