{{Rsnum
|rsid=35685286
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226933
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35685286
|variant=0161
}}

{{ClinVar
|rsid=35685286
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5248163
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248163C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016460.1
|CLNDBN=HEMOGLOBIN LUFKIN
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=288; 141900.0161
|Disease=HEMOGLOBIN LUFKIN
}}

{{PMID Auto
|PMID=24022
|Title=Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residue.
}}

{{PMID Auto
|PMID=8537234
|Title=Hb S-Hb Lufkin disease in a black male infant.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}