{{Rsnum
|rsid=35849199
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5225705
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35849199
|variant=0117
}}

{{ClinVar
|rsid=35849199
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5246935
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246935A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016392.1; RCV000016393.24
|CLNDBN=HEMOGLOBIN INDIANAPOLIS; Heinz body hemolytic anemia
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0117
|Disease=HEMOGLOBIN INDIANAPOLIS; Heinz body hemolytic anemia
}}

{{PMID Auto
|PMID=429365
|Title=The structure of hemoglobin Indianapolis [beta112(G14) arginine]. An unstable variant detectable only by isotopic labeling.
}}

{{PMID Auto
|PMID=447835
|Title=Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
|OA=1
}}

{{PMID Auto
|PMID=3781865
|Title=A case of hemoglobin Indianapolis [beta 112(G14) Cys----Arg] in an individual from Cordoba, Spain.
}}

{{on chip | 23andMe v3}}