{{Rsnum
|rsid=77656691
|Chromosome=4
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ALB
|position=73409474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77656691
|variant=0048
}}{{ClinVar
|rsid=77656691
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=74275191
|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.74275191G>T
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019875.1
|CLNDBN=ALBUMIN HAWKES BAY
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0048
|Disease=ALBUMIN HAWKES BAY
}}{{PMID Auto
|PMID=8347685
|Title=Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177.
}}