{{Rsnum
|rsid=33994623
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226780
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33994623
|variant=0241
}}
{{omim
|id=141900
|rsnum=33994623
|variant=0440
}}{{ClinVar
|rsid=33994623
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248010
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 3
|CLNHGVS=NC_000011.9:g.5248010A>C; NC_000011.9:g.5248010A>T
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016794.1; RCV000016571.1
|CLNDBN=HEMOGLOBIN HOWICK; HEMOGLOBIN ROTHSCHILD
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0440; 141900.0241
|Disease=HEMOGLOBIN HOWICK; HEMOGLOBIN ROTHSCHILD
}}{{PMID Auto
|PMID=913596
|Title=Structural and functional studies of Hb Rothschild beta (C3) Trp replaced by Arg. A new variant of the alpha1beta2 contact.
}}

{{PMID Auto
|PMID=7068435
|Title=Hb Rothschild (beta 37 (C2) Trp leads to Arg): clinical studies.
}}

{{PMID Auto
|PMID=7391018
|Title=Refolding defects in hemoglobin Rothschild.
}}

{{PMID Auto
|PMID=8144352
|Title=Hb Howick [beta 37(C3)Trp-->Gly]: a new high oxygen affinity variant of the alpha 1 beta 2 contact.
}}