{{Rsnum
|rsid=77238412
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ALB
|position=73408735
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77238412
|variant=0006
}}{{ClinVar
|rsid=77238412
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=74274452
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000040002110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74274452C>G
|CLNORIGIN=0
|CLNSRCID=
103600.0006
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000019830.1
|Tags=PM;PMC;S3D;VLD;OTHERKG;LSD;OM
|CLNDBN=ALBUMIN YANOMAMA 2
|CLNSRC=OMIM Allelic Variant
|Disease=ALBUMIN YANOMAMA 2
}}{{PMID Auto
|PMID=3479777
|Title=Amino acid substitutions in inherited albumin variants from Amerindian and Japanese populations.
|OA=1
}}

{{PMID Auto
|PMID=6496475
|Title=Bilirubin binding by variant albumins in Yanomama Indians.
|OA=1
}}

{{PMID Auto
|PMID=7937781
|Title=Analbuminemia: three cases resulting from different point mutations in the albumin gene.
|OA=1
}}

{{PMID Auto
|PMID=15996651
|Title=Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene.
}}