{{Rsnum
|rsid=79047363
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73416262
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=79047363
|variant=0017
}}
{{omim
|id=103600
|rsnum=79047363
|variant=0052
}}{{ClinVar
|rsid=79047363
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=74281979
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000004.11:g.74281979G>A; NC_000004.11:g.74281979G>C
|CLNORIGIN=0
|CLNSRCID=
103600.0017; 103600.0052
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000019847.1; RCV000019896.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDBN=ALBUMIN TOCHIGI; ALBUMIN MALMO 5
|CLNSRC=OMIM Allelic Variant
|Disease=ALBUMIN TOCHIGI; ALBUMIN MALMO 5
}}{{PMID Auto
|PMID=2762316
|Title=Point substitutions in Japanese alloalbumins.
|OA=1
}}

{{PMID Auto
|PMID=1518850
|Title=Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.
|OA=1
}}