{{Rsnum
|rsid=75523493
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73418232
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=75523493
|variant=0019
}}{{ClinVar
|rsid=75523493
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=74283949
|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.74283949G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019849.1; RCV000019850.1; RCV000019851.1; RCV000019852.1; RCV000019853.1; RCV000019854.1
|CLNDBN=ALBUMIN LAMBADI; ALBUMIN MANAUS-1; ALBUMIN VANCOUVER; ALBUMIN BIRMINGHAM; ALBUMIN ADANA; ALBUMIN PORTO ALEGRE 2
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0019
|Disease=ALBUMIN LAMBADI; ALBUMIN MANAUS-1; ALBUMIN VANCOUVER; ALBUMIN BIRMINGHAM; ALBUMIN ADANA; ALBUMIN PORTO ALEGRE 2
}}{{PMID Auto
|PMID=2317208
|Title=Genetic characterization of an alloalbumin, albumin Kashmir, using gene amplification and allele-specific oligonucleotides.
|OA=1
}}

{{PMID Auto
|PMID=2404284
|Title=Point substitutions in albumin genetic variants from Asia.
|OA=1
}}