Canonical Allele Identifier: CA444396984

Gene: CCNO

Linked Data

• dbSNP Id: rs1346814165
• gnomAD v3: 5-55233287-A-T
• gnomAD v4: 5-55233287-A-T
• MyVariant Identifiers: chr5:g.54529115A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233287A>T , CM000667.2:g.55233287A>T	GRCh38
NC_000005.9:g.54529115A>T , CM000667.1:g.54529115A>T	GRCh37
NC_000005.8:g.54564872A>T	NCBI36
NG_034201.1:g.5431T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.237T>A MANE Select	ENSP00000282572.4:p.Gly79=
ENST00000282572.4:c.237T>A	ENSP00000282572.4:p.Gly79=
ENST00000501463.2:c.237T>A	ENSP00000422485.1:p.Gly79=
NM_021147.4:c.237T>A	NP_066970.3:p.Gly79=
NR_125346.1:n.431T>A
NR_125347.1:n.431T>A
NM_021147.5:c.237T>A MANE Select	NP_066970.3:p.Gly79=
NR_125346.2:n.322T>A
NR_125347.2:n.322T>A