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SNP ID:
rs6600143
Gene
HBZ
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.16: 151390 - 151390 on Build GRCh38
Polymorphism:
A/C, Transversion substitution
Context Sequence [VIC/FAM]:

TATCTGACAAGGGATTGCTTCCAGA[A/C]GATACACAGAATTCTAAAAATTCAT

Assay ID C__31076414_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 142310

Literature Links:

 HBZ PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.19)
(0.81)
Caucasian - Not Available CEPH (CEU)
C (0.31)
(0.69)
EAS
C (0.26)
(0.74)
African American - Not Available YRI (Yoruba) - Not Available
SAS
C (0.24)
(0.76)
Chinese - Not Available JPT (Japanese)
C (0.25)
(0.75)
AFR
C (0.01)
(0.99)
Japanese - Not Available CHB (Han Chinese)
C (0.40)
(0.60)
EUR
C (0.30)
(0.70)
AMR
C (0.19)
(0.81)
HBZ - hemoglobin subunit zeta
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_005332.2 Intron NP_005323.1
XM_005255287.3 Intron XP_005255344.1
XM_005255288.3 Intron XP_005255345.1

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