{{Rsnum
|rsid=33926796
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226767
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33926796
|variant=0174
}}
{{omim
|id=141900
|rsnum=33926796
|variant=0441
}}
{{omim
|id=141900
|rsnum=33926796
|variant=0511
}}{{ClinVar
|rsid=33926796
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5247997
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5247997A>C; NC_000011.9:g.5247997A>G; NC_000011.9:g.5247997A>T
|CLNORIGIN=1
|CLNSRCID=
1119; 141900.0511; 313; 141900.0441; 312; 141900.0174
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016865.1; RCV000016795.1; RCV000016488.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN ILMENAU; HEMOGLOBIN DENVER; HEMOGLOBIN MEQUON
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN ILMENAU; HEMOGLOBIN DENVER; HEMOGLOBIN MEQUON
}}{{PMID Auto
|PMID=974262
|Title=Hemoglobin M equon beta 41 (C7) phenylalanine leads to tyrosine.
}}

{{PMID Auto
|PMID=8133661
|Title=Hemoglobin Denver [alpha 2 beta 2(41) (C7) Phe-->Ser]: a low-O2-affinity variant associated with chronic cyanosis and anemia.
}}

{{PMID Auto
|PMID=12144060
|Title=A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [beta41 (C7)Phe-->Cys].
}}