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Search Thermo Fisher Scientific
AGGGATTACCGTTCTTCACGGGATT[C/T]AGCCCTGGCGTCTTGCCTAGGGCGT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109480 | |||||||||||||||||||||||
Literature Links: |
BSG PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
BSG - basigin (Ok blood group) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322243.1 | Intron | NP_001309172.1 | ||||
NM_001728.3 | Intron | NP_001719.2 | ||||
NM_198589.2 | Intron | NP_940991.1 | ||||
NM_198590.2 | Intron | NP_940992.1 | ||||
NM_198591.2 | Intron | NP_940993.1 | ||||
XM_017027173.1 | Intron | XP_016882662.1 |
Set Membership: |
HapMap |