{{Rsnum
|rsid=77335374
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73411994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77335374
|variant=0027
}}{{ClinVar
|rsid=77335374
|Reversed=0
|FwdREF=A
|FwdALT=G,T
|REF=A
|ALT=G,T
|RSPOS=74277711
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000502110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74277711A>G
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000019869.26
|CLNDBN=Analbuminemia, american indian type
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0027
|Disease=Analbuminemia
}}{{PMID Auto
|PMID=3353369
|Title=Splicing mutation in human hereditary analbuminemia.
|OA=1
}}