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- SNP ID:
- rs141494605
- Gene
-
HBA2HBM - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.16: 166594 - 166594 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TTCTCCTGCAGCTGCTAATCCAGTG[C/T]TTCCACGTCGTGCTGGCCTCCCACC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 141850
MIM: 609639
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Literature Links: |
HBA2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
| HBA2 - hemoglobin subunit alpha 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| HBM - hemoglobin subunit mu | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001003938.3 | 336 | Silent Mutation | TGC,TGT | C,C 104 | NP_001003938.1 | |
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