{{Rsnum
|rsid=33971634
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5225660
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33971634
|variant=0027
}}
{{omim
|id=141900
|rsnum=33971634
|variant=0096
}}{{ClinVar
|rsid=33971634
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=5246890
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2; 3
|CLNHGVS=NC_000011.9:g.5246890G>C; NC_000011.9:g.5246890G>T
|CLNORIGIN=1
|CLNSRCID=
522; 141900.0096; 523; 141900.0027
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016366.1; RCV000016367.1; RCV000016270.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN HACETTEPE; HEMOGLOBIN COMPLUTENSE; HEMOGLOBIN BREST
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN HACETTEPE; HEMOGLOBIN COMPLUTENSE; HEMOGLOBIN BREST
}}{{PMID Auto
|PMID=938658
|Title=Hemoglobin Hacettepe or alpha 2 beta 2 127 (H5) Gln replaced by Glu.
}}

{{PMID Auto
|PMID=3660178
|Title=[Hemoglobin Complutense (beta 127 (H5) Gln replaced by Glu) in a Spanish family].
}}

{{PMID Auto
|PMID=3707969
|Title=Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification.
}}

{{PMID Auto
|PMID=3384710
|Title=Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior.
}}

{{PMID Auto
|PMID=1958498
|Title=A novel mutation (nonsense beta 127) in exon 3 of the beta globin gene produces a variable thalassaemic phenotype.
}}