{{Rsnum
|rsid=33912272
|Gene=HBB
|Chromosome=11
|position=5227006
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33912272
|variant=0451
}}{{ClinVar
|rsid=33912272
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=5248236
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000116110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248236G>A
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591; .
|COMMON=0
|CLNACC=RCV000016806.1
|CLNDBN=HEMOGLOBIN TYNE
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=225; 141900.0451
|Disease=HEMOGLOBIN TYNE
}}{{PMID Auto
|PMID=7852088
|Title=A new beta chain variant, Hb Tyne [beta 5(A2)Pro-->Ser].
}}

{{PMID Auto
|PMID=12507970
|Title=Hemoglobin Gorwihl [alpha2beta(2)5(A2)Pro-->Ala], an electrophoretically silent variant with impaired glycation.
}}

{{PMID Auto
|PMID=20353350
|Title=Relationship between impaired glycation and the N-terminal structure of the Hb Gorwihl [beta5(A2)Pro-->Ala] variant.
}}