{{Rsnum
|rsid=33946157
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226976
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33946157
|variant=0019
}}
{{omim
|id=141900
|rsnum=33946157
|variant=0234
}}{{ClinVar
|rsid=33946157
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248206
|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.5248206A>C; NC_000011.9:g.5248206A>T
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016564.1; RCV000016261.1
|CLNDBN=HEMOGLOBIN RANDWICK; HEMOGLOBIN BELFAST
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0234; 141900.0019
|Disease=HEMOGLOBIN RANDWICK; HEMOGLOBIN BELFAST
}}{{PMID Auto
|PMID=821297
|Title=A 2d case of haemoglobin Belfast (beta 15 (A 12) Trp replaced by Arg) observed in a French patient.
}}

{{PMID Auto
|PMID=4434089
|Title=Haemoglobin Belfast 15 (A12) tryptophan leading to arginine: a new unstable haemoglobin variant.
|OA=1
}}

{{PMID Auto
|PMID=6814990
|Title=Hb Belfast (beta 15 (A 12) Trp leads to Arg) in combination with G6PD deficiency in an Italian carrier.
}}

{{PMID Auto
|PMID=7141875
|Title=Hb Belfast (beta 15 Trp replaced by Arg) in an Italian family.
}}

{{PMID Auto
|PMID=15481889
|Title=Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype.
}}

{{PMID Auto
|PMID=3384707
|Title=Hemoglobin Randwick or beta 15 (A12)Trp----Gly: a new unstable beta-chain hemoglobin variant.
}}