{{Rsnum
|rsid=79738788
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73419575
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=79738788
|variant=0021
}}{{ClinVar
|rsid=79738788
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=74285292
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000004.11:g.74285292A>G
|CLNORIGIN=0
|CLNSRCID=
103600.0021
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000019857.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDBN=ALBUMIN MEXICO 2
|CLNSRC=OMIM Allelic Variant
|Disease=ALBUMIN MEXICO 2
}}{{PMID Auto
|PMID=3474609
|Title=Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning.
|OA=1
}}

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