SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 240
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs34034824

Organism human (Homo sapiens)
Variation Class DIP: deletion/insertion polymorphism
Alleles -/G
Orientation fwd/
Chr-Number 11
SNP type N
Length 601
5' Near Seq 30 bp tgcgtctccagaatatgcaaaatacttaca
3' Near Seq 30 bp ggacagaatggatgaaaactctacctcagt
Fasta Sequence CTTCTGGCAC TGGCTTAGGA GTTGGACTTC AAACCCTCAG CCCTCCCTCT AAGATATATC TCTTGGCCCC ATACCATCAG TACAAATTGC TACTAAAAAC ATCCTCCTTT GCAAGTGTAT TTACGTAATA TTTGGAATCA CAGCTTGGTA AGCATATTGA AGATCGTTTT CCCAATTTTC TTATTACACA AATAAGAAGT TGATGCACTA AAAGTGGAAG AGTTTTGTCT ACCATAATTC AGCTTTGGGA TATGTAGATG GATCTCTTCC TGCGTCTCCA GAATATGCAA AATACTTACA N GGACAGAATG GATGAAAACT CTACCTCAGT TCTAAGCATA TCTTCTCCTT ATTTGGATTA AAACCTTCTG GTAAGAAAAG AAAAAAAAAT ATATATATAT ATGTGTATAT ATACACACAT ACATATACAT ATATATGCAT TCATTTGTTG TTGTTTTTCT TAATTTGCTC ATGCATGCTA ATAAATTATG TCTAAAAATA GAATAAATAC AAATCAATGT GCTCTGTGCA TTAGTTACTT ATTAGGTTTT GGGAAACAAG AGATAAAAAA CTAGAGACCT CTTAATGCAG TCAAAAATAC
     

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