{{Rsnum
|rsid=33918343
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226689
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33918343
|variant=0163
}}
{{omim
|id=141900
|rsnum=33918343
|variant=0274
}}
{{omim
|id=141900
|rsnum=33918343
|variant=0438
}}{{ClinVar
|rsid=33918343
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5247919
|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.5247919A>C; NC_000011.9:g.5247919A>G; NC_000011.9:g.5247919A>T
|CLNORIGIN=1
|CLNSRCID=
372; 141900.0438; 371; 141900.0274; 368; 141900.0163
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016792.1; RCV000016615.1; RCV000016462.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN MANUKAU; HEMOGLOBIN SYDNEY; HEMOGLOBIN M (MILWAUKEE 1)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN MANUKAU; HEMOGLOBIN SYDNEY; HEMOGLOBIN M (MILWAUKEE 1)
}}{{PMID Auto
|PMID=4311041
|Title=Properties of hemoglobin M, Milwaukee-I variant and its unique characteristic.
}}

{{PMID Auto
|PMID=5420327
|Title=Some observations on the properties of hemoglobin M Milwaukee-1.
}}

{{PMID Auto
|PMID=6050213
|Title=Haemoglobin sydney: Beta-67 (E11) valine modified to alanine: an emerging pattern of unstable haemoglobins.
}}

{{PMID Auto
|PMID=8280608
|Title=Haemoglobin Manukau beta 67[E11] Val-->Gly: transfusion-dependent haemolytic anaemia ameliorated by coexisting alpha thalassaemia.
}}