{{Rsnum
|rsid=76587671
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73419613
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=76587671
|variant=0022
}}{{ClinVar
|rsid=76587671
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=74285330
|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
|CLNHGVS=NC_000004.11:g.74285330G>A
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019858.1
|CLNDBN=ALBUMIN FUKUOKA 1
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0022
|Disease=ALBUMIN FUKUOKA 1
}}{{PMID Auto
|PMID=2404284
|Title=Point substitutions in albumin genetic variants from Asia.
|OA=1
}}

{{PMID Auto
|PMID=9392528
|Title=Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.
}}