{{Rsnum
|rsid=77158239
|Chromosome=4
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ALB
|position=73420278
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77158239
|variant=0032
}}{{ClinVar
|rsid=77158239
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=TC
|ALT=T
|RSPOS=74285994
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110200
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74285995delC
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019876.1; RCV000019877.1
|CLNDBN=ALBUMIN GE/CT; ALBUMIN CATANIA
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0032
|Disease=ALBUMIN GE/CT; ALBUMIN CATANIA
}}{{PMID Auto
|PMID=2068071
|Title=A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.
|OA=1
}}

{{PMID Auto
|PMID=3081519
|Title=Structural characterization of a chain termination mutant of human serum albumin.
}}