{{Rsnum
|rsid=41479347
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173540
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141800
|rsnum=41479347
|variant=0156
}}{{ClinVar
|rsid=41479347
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=223539
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223539C>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017178.1
|CLNDBN=HEMOGLOBIN WESTMEAD
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0156
|Disease=HEMOGLOBIN WESTMEAD
}}

{{PMID Auto
|PMID=1686260
|Title=Hb Westmead: an alpha 2-globin gene mutation detected by polymerase chain reaction and Stu I cleavage.
}}

{{PMID Auto
|PMID=1787098
|Title=Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family.
}}

{{PMID Auto
|PMID=6153381
|Title=Hemoglobin Westmead alpha 2 122(H5)His replaced by Gln beta 2: a new hemoglobin variant with the substitution in the alpha 1 beta 1 contact area.
}}

{{PMID Auto
|PMID=15182058
|Title=Thalassemia intermedia due to co-inheritance of beta0/beta(+)-thalassemia and (- -SEA) alpha-thalassemia/Hb Westmead [alpha122(H5)His > Gln (alpha2)] in a Chinese family.
}}

{{on chip | 23andMe v4}}