|
|
| 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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