{{Rsnum
|rsid=387907182
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALG11
|position=52024872
|Gene_s=ALG11,UTP14C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=13
|CLNACC=RCV000024341.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1P
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C3150913:613661:280071
|CLNHGVS=NC_000013.10:g.52599008T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613666.0004
|Disease=Congenital disorder of glycosylation type 1P
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=52599008
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907182
|GENEINFO=ALG11:440138; UTP14C:9724
|GENE_ID=440138; 9724
|GENE_NAME=ALG11; UTP14C
}}