{{Rsnum
|rsid=80338677
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MAN2B1
|position=12655693
|Gene_s=MAN2B1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=19
|CLNACC=RCV000020364.1
|CLNALLE=1
|CLNDBN=Deficiency of alpha-mannosidase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1396:C0024748:248500:61:124466001
|CLNHGVS=NC_000019.9:g.12766507C>G
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1396
|Disease=Deficiency of alpha-mannosidase
|FwdALT=C
|FwdREF=G
|GENEINFO=MAN2B1:4125
|GENE_ID=4125
|GENE_NAME=MAN2B1
|REF=C
|RSPOS=12766507
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80338677
}}{{PMID Auto
|PMID=9915946
|Title=Spectrum of mutations in alpha-mannosidosis.
|OA=1
}}