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- SNP ID:
- rs753092900
- Gene
-
ALPL - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 21567733 - 21567733 on Build GRCh38
- Polymorphism:
- T/C, Transition substitution
- Context Sequence [VIC/FAM]:
TGGAAAACAGGTGGCCAGGGTTTAT[T/C]GCAGCCTTGGTATGAAGTTGAGTCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 171760
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Literature Links: |
ALPL PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| 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 |
| ALPL - alkaline phosphatase, liver/bone/kidney | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000478.5 | Intron | NP_000469.3 | ||||
| NM_001127501.3 | Intron | NP_001120973.2 | ||||
| NM_001177520.2 | Intron | NP_001170991.1 | ||||
| XM_005245818.1 | Intron | XP_005245875.1 | ||||
| XM_006710546.2 | Intron | XP_006710609.1 | ||||
| XM_017000903.1 | Intron | XP_016856392.1 | ||||
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