{{Rsnum
|rsid=75152012
|Chromosome=4
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=ALB
|position=73406719
|Gene_s=ALB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=75152012
|Reversed=0
|FwdREF=AT
|FwdALT=
|REF=CAT
|ALT=C
|RSPOS=74272435
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=0
|VP=0x050268001201000002110200
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74272436_74272437delAT
|CLNORIGIN=0
|CLNSIG=1
|CLNCUI=103600
|CLNDBN=OMIM
|Tags=PM;PMC;S3D;NSF;REF;OTHERKG;LSD;OM
}}{{PMID|12028999}} Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families.

{{PMID|16183048}} Analbuminemia in a Slovak Romany (gypsy) family: case report and mutational analysis.

{{PMID|17952464}} A boy with congenital analbuminemia and steroid-sensitive idiopathic nephrotic syndrome: an experiment of nature.

{{PMID|18602380}} Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT).

{{PMID|18791744}} Congenital analbuminemia with acute glomerulonephritis: a diagnostic challenge.