Canonical Allele Identifier: CA1547396548

Gene: CCNO

Linked Data

• dbSNP Id: rs1305200929
• gnomAD v4: 5-55232931-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232931G>A , CM000667.2:g.55232931G>A	GRCh38
NC_000005.9:g.54528759G>A , CM000667.1:g.54528759G>A	GRCh37
NC_000005.8:g.54564516G>A	NCBI36
NG_034201.1:g.5787C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+212C>T MANE Select	ENSP00000282572.4:n.381+212C>T
ENST00000282572.4:c.381+212C>T	ENSP00000282572.4:n.381+212C>T
ENST00000501463.2:c.*197C>T	ENSP00000422485.1:n.*197C>T
NM_021147.4:c.381+212C>T	NP_066970.3:n.381+212C>T
NR_125346.1:n.787C>T
NR_125347.1:n.580+207C>T
NR_125348.1:n.61C>T
NM_021147.5:c.381+212C>T MANE Select	NP_066970.3:n.381+212C>T
NR_125346.2:n.678C>T
NR_125347.2:n.471+207C>T