Assay Details
Target Gene Details
Entrez Gene ID: | 3170 |
Gene Name: | forkhead box A2 |
Gene Aliases: |
HNF3B, TCF3B |
Location: |
Chr.20:22581004-22585463 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FOXA2 | NM_021784.4 | 2 | 1497 | NP_068556.2 |
| NM_153675.2 | 3 | 1484 | NP_710141.1 | |
| AB028021.1 | 3 | 1490 | BAA78106.1 | |
| AI302734.1 | ||||
| AK301611.1 | 3 | 955 | ||
| BC006545.2 | 2 | 1290 | AAH06545.2 | |
| BC011780.2 | 2 | 1336 | AAH11780.1 | |
| BC019288.1 | 2 | 1290 | AAH19288.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv953003 | Chr.20:22575463 - 22586762 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs149455805] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
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Genomic Map