Canonical Allele Identifier: CA118945795

Gene: CCNO

Linked Data

• dbSNP Id: rs945769096
• gnomAD v2: 5-54529478-C-T
• gnomAD v3: 5-55233650-C-T
• gnomAD v4: 5-55233650-C-T
• MyVariant Identifiers: chr5:g.54529478C>T (hg19) ; chr5:g.55233650C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233650C>T , CM000667.2:g.55233650C>T	GRCh38
NC_000005.9:g.54529478C>T , CM000667.1:g.54529478C>T	GRCh37
NC_000005.8:g.54565235C>T	NCBI36
NG_034201.1:g.5068G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-127G>A	ENSP00000282572.4:n.-127G>A
NM_021147.4:c.-127G>A	NP_066970.3:n.-127G>A
NR_125346.1:n.68G>A
NR_125347.1:n.68G>A