Canonical Allele Identifier: CA607271219

Gene: UNG

Linked Data

• dbSNP Id: rs949986283
• gnomAD v2: 12-109538162-C-A
• gnomAD v3: 12-109100357-C-A
• gnomAD v4: 12-109100357-C-A
• MyVariant Identifiers: chr12:g.109538162C>A (hg19) ; chr12:g.109100357C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109100357C>A , CM000674.2:g.109100357C>A	GRCh38
NC_000012.11:g.109538162C>A , CM000674.1:g.109538162C>A	GRCh37
NC_000012.10:g.108022545C>A	NCBI36
NG_007284.1:g.7748C>A , LRG_124:g.7748C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000539287.6:c.408+1073C>A	ENSP00000440784.1:n.408+1073C>A
ENST00000699559.1:c.408+1073C>A	ENSP00000514433.1:n.408+1073C>A
ENST00000699560.1:c.313-1545C>A	ENSP00000514434.1:n.313-1545C>A
ENST00000699561.1:c.408+1073C>A	ENSP00000514435.1:n.408+1073C>A
ENST00000699562.1:c.408+1073C>A	ENSP00000514436.1:n.408+1073C>A
ENST00000699563.1:c.408+1073C>A	ENSP00000514437.1:n.408+1073C>A
ENST00000699564.1:c.408+1073C>A	ENSP00000514438.1:n.408+1073C>A
ENST00000699565.1:c.408+1073C>A	ENSP00000514439.1:n.408+1073C>A
ENST00000699566.1:c.513+1073C>A	ENSP00000514440.1:n.513+1073C>A
ENST00000699567.1:c.408+1073C>A	ENSP00000514441.1:n.408+1073C>A
ENST00000242576.7:c.435+1073C>A MANE Select	ENSP00000242576.3:n.435+1073C>A
ENST00000242576.6:c.435+1073C>A	ENSP00000242576.2:n.435+1073C>A
ENST00000336865.6:c.408+1073C>A	ENSP00000337398.2:n.408+1073C>A
ENST00000446767.2:c.408+1073C>A	ENSP00000400287.2:n.408+1073C>A
ENST00000539287.5:c.408+1073C>A	ENSP00000440784.1:n.408+1073C>A
NM_003362.3:c.408+1073C>A	NP_003353.1:n.408+1073C>A
NM_080911.2:c.435+1073C>A	NP_550433.1:n.435+1073C>A
NM_003362.4:c.408+1073C>A	NP_003353.1:n.408+1073C>A
NM_080911.3:c.435+1073C>A MANE Select	NP_550433.1:n.435+1073C>A