{{Rsnum
|rsid=34703513
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5226776
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34703513
|variant=0461
}}{{ClinVar
|rsid=34703513
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=5248006
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5248006G>A; NC_000011.9:g.5248006G>T
|CLNORIGIN=1
|CLNSRCID=
141900.0537; 141900.0461
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016889.1; RCV000016815.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN LA CORUNA; HEMOGLOBIN HINWIL
|CLNSRC=OMIM Allelic Variant
|Disease=HEMOGLOBIN LA CORUNA; HEMOGLOBIN HINWIL
}}{{PMID Auto
|PMID=8745430
|Title=HB Hinwil or beta 38(C4)Thr-->Asn: a new beta chain variant detected in a Swiss family.
}}

{{PMID Auto
|PMID=16840229
|Title=Hb La Coruna [beta38(C4)Thr-->Ile]: a new hemoglobin variant leading to familial polycythemia.
}}