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CTCGGGGCAGGCTGAGCGGGGGCAC[C/G]GCATAGGGGAGGGAGGACACGTTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607759 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGA2B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ITGA2B - integrin subunit alpha 2b | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000419.4 | 3035 | Silent Mutation | GCC,GCG | A,A 969 | NP_000410.2 | |
XM_011524749.1 | 3035 | Intron | XP_011523051.1 | |||
XM_011524750.1 | 3035 | Silent Mutation | GCC,GCG | A,A 969 | XP_011523052.1 |