Canonical Allele Identifier: CA812219151

Gene: CCNO

Linked Data

• dbSNP Id: rs1229718760
• gnomAD v3: 5-55233627-G-A
• gnomAD v4: 5-55233627-G-A
• MyVariant Identifiers: chr5:g.54529455G>A (hg19) ; chr5:g.55233627G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233627G>A , CM000667.2:g.55233627G>A	GRCh38
NC_000005.9:g.54529455G>A , CM000667.1:g.54529455G>A	GRCh37
NC_000005.8:g.54565212G>A	NCBI36
NG_034201.1:g.5091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-104C>T	ENSP00000282572.4:n.-104C>T
NM_021147.4:c.-104C>T	NP_066970.3:n.-104C>T
NR_125346.1:n.91C>T
NR_125347.1:n.91C>T