{{Rsnum
|rsid=34378160
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226764
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34378160
|variant=0100
}}

{{ClinVar
|rsid=34378160
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=5247994
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5247994A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016371.1; RCV000016372.1; RCV000016373.24
|CLNDBN=HEMOGLOBIN HAMMERSMITH; HEMOGLOBIN CHIBA; Heinz body hemolytic anemia
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0100
|Disease=HEMOGLOBIN HAMMERSMITH; HEMOGLOBIN CHIBA; Heinz body hemolytic anemia
}}

{{PMID Auto
|PMID=1201210
|Title=The oxygen affinity of haemoglobin Hammersmith.
}}

{{PMID Auto
|PMID=1634359
|Title=The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA.
}}

{{PMID Auto
|PMID=6082463
|Title=Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser).
}}

{{PMID Auto
|PMID=9856680
|Title=Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies.
}}

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