Canonical Allele Identifier: CA1076233606

Gene: CCNO

Linked Data

• dbSNP Id: rs1745636843
• gnomAD v3: 5-55232932-G-A
• gnomAD v4: 5-55232932-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232932G>A , CM000667.2:g.55232932G>A	GRCh38
NC_000005.9:g.54528760G>A , CM000667.1:g.54528760G>A	GRCh37
NC_000005.8:g.54564517G>A	NCBI36
NG_034201.1:g.5786C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+211C>T MANE Select	ENSP00000282572.4:n.381+211C>T
ENST00000282572.4:c.381+211C>T	ENSP00000282572.4:n.381+211C>T
ENST00000501463.2:c.*196C>T	ENSP00000422485.1:n.*196C>T
NM_021147.4:c.381+211C>T	NP_066970.3:n.381+211C>T
NR_125346.1:n.786C>T
NR_125347.1:n.580+206C>T
NR_125348.1:n.60C>T
NM_021147.5:c.381+211C>T MANE Select	NP_066970.3:n.381+211C>T
NR_125346.2:n.677C>T
NR_125347.2:n.471+206C>T