Canonical Allele Identifier: CA812218058

Gene: CCNO

Linked Data

• dbSNP Id: rs1364654232
• gnomAD v3: 5-55232913-C-A
• gnomAD v4: 5-55232913-C-A
• MyVariant Identifiers: chr5:g.54528741C>A (hg19) ; chr5:g.55232913C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232913C>A , CM000667.2:g.55232913C>A	GRCh38
NC_000005.9:g.54528741C>A , CM000667.1:g.54528741C>A	GRCh37
NC_000005.8:g.54564498C>A	NCBI36
NG_034201.1:g.5805G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+230G>T MANE Select	ENSP00000282572.4:n.381+230G>T
ENST00000282572.4:c.381+230G>T	ENSP00000282572.4:n.381+230G>T
ENST00000501463.2:c.*215G>T	ENSP00000422485.1:n.*215G>T
NM_021147.4:c.381+230G>T	NP_066970.3:n.381+230G>T
NR_125346.1:n.805G>T
NR_125347.1:n.580+225G>T
NR_125348.1:n.79G>T
NM_021147.5:c.381+230G>T MANE Select	NP_066970.3:n.381+230G>T
NR_125346.2:n.696G>T
NR_125347.2:n.471+225G>T