{{Rsnum
|rsid=387906277
|Chromosome=11
|position=78121130
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ALG8
|Gene_s=ALG8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000002667.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1H
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C1842539:608104:79325
|CLNHGVS=NC_000011.9:g.77832176delG
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608103.0001
|Disease=Congenital disorder of glycosylation type 1H
|FwdREF=C
|REF=TG
|RSPOS=77832175
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906277
|GENEINFO=ALG8:79053
|GENE_ID=79053
|GENE_NAME=ALG8
}}