Canonical Allele Identifier: CA3266884

Gene: CCNO

Linked Data

• dbSNP Id: rs776186988
• ExAC: 5:54529355 G / T
• gnomAD v2: 5-54529355-G-T
• gnomAD v4: 5-55233527-G-T
• MyVariant Identifiers: chr5:g.54529355G>T (hg19) ; chr5:g.55233527G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233527G>T , CM000667.2:g.55233527G>T	GRCh38
NC_000005.9:g.54529355G>T , CM000667.1:g.54529355G>T	GRCh37
NC_000005.8:g.54565112G>T	NCBI36
NG_034201.1:g.5191C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.-4C>A MANE Select	ENSP00000282572.4:n.-4C>A
ENST00000282572.4:c.-4C>A	ENSP00000282572.4:n.-4C>A
ENST00000501463.2:c.-4C>A	ENSP00000422485.1:n.-4C>A
NM_021147.4:c.-4C>A	NP_066970.3:n.-4C>A
NR_125346.1:n.191C>A
NR_125347.1:n.191C>A
NM_021147.5:c.-4C>A MANE Select	NP_066970.3:n.-4C>A
NR_125346.2:n.82C>A
NR_125347.2:n.82C>A