Canonical Allele Identifier: CA812219154

Gene: CCNO

Linked Data

• dbSNP Id: rs231623
• gnomAD v4: 5-55233630-C-A
• MyVariant Identifiers: chr5:g.54529458C>A (hg19) ; chr5:g.55233630C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233630C>A , CM000667.2:g.55233630C>A	GRCh38
NC_000005.9:g.54529458C>A , CM000667.1:g.54529458C>A	GRCh37
NC_000005.8:g.54565215C>A	NCBI36
NG_034201.1:g.5088G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-107G>T	ENSP00000282572.4:n.-107G>T
NM_021147.4:c.-107G>T	NP_066970.3:n.-107G>T
NR_125346.1:n.88G>T
NR_125347.1:n.88G>T