SNP Browser for Human [Homo spaiens] Genetic Disorders

  Home
  About us
  About Database
  SNPs ?
  Genetic Disorders ?
  Genetic Disorder List
  Genes List
  SNP Registry
  Acknowledgement
  References
  Our Team
  Contact us


ID 247
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs2156920

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/B
Chr-Number 11
SNP type S
Length 510
5' Near Seq 30 bp ttaaaaagaagaaaatcctgccatttatgc
3' Near Seq 30 bp agaattgatgaacctggaggatgtaaaact
Fasta Sequence GGaaaaataa agaagtgagg ctacatcaaa ctaaaaaatt tccacacaaa aaagaaaaca atgaacaaat gaaaggtgaa ccatgaaatg gcatatttgc aaaccaaata tttcttaaat attttggtta atatccaaaa tatataagaa acacagatga ttcaataaca aacaaaaaat taaAAATAGG AAAATAAAAA Aattaaaaag aagaaaatcc tgccatttat gc S agaattgatg aacctggagg atgtaaaact aagaaaaata agcctgacac aaaaagacaa atactacaca accttgctca tatgtgaaac ataaaaaagt cactctcatg gaaacagaca gtagaggtat ggtttccagg ggttgggggt gggagaatca ggaaactatt actcaaaggg tataaaattt cagttatgtg ggatgaataa attctagata tctaatgtac agcatcgtga ctgtagttaa ttgtactgta agtatattta aaatttg
     

© 2008, IBI Biosolutions Pvt Ltd. INDIA