Canonical Allele Identifier: CA812218103

Gene: CCNO

Linked Data

• dbSNP Id: rs1343457117
• gnomAD v3: 5-55232978-A-C
• gnomAD v4: 5-55232978-A-C
• MyVariant Identifiers: chr5:g.54528806A>C (hg19) ; chr5:g.55232978A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232978A>C , CM000667.2:g.55232978A>C	GRCh38
NC_000005.9:g.54528806A>C , CM000667.1:g.54528806A>C	GRCh37
NC_000005.8:g.54564563A>C	NCBI36
NG_034201.1:g.5740T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+165T>G MANE Select	ENSP00000282572.4:n.381+165T>G
ENST00000282572.4:c.381+165T>G	ENSP00000282572.4:n.381+165T>G
ENST00000501463.2:c.*150T>G	ENSP00000422485.1:n.*150T>G
NM_021147.4:c.381+165T>G	NP_066970.3:n.381+165T>G
NR_125346.1:n.740T>G
NR_125347.1:n.580+160T>G
NR_125348.1:n.14T>G
NM_021147.5:c.381+165T>G MANE Select	NP_066970.3:n.381+165T>G
NR_125346.2:n.631T>G
NR_125347.2:n.471+160T>G