Assay Details
Target Gene Details
Entrez Gene ID: | 10949 |
Gene Name: | heterogeneous nuclear ribonucleoprotein A0 |
Gene Aliases: |
HNRPA0 |
Location: |
Chr.5:137751384-137754350 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HNRNPA0 | NM_006805.3 | 1 | 1939 | NP_006796.1 |
| AA081021.1 | 1 | 310 | ||
| AA442538.1 | 1 | 102 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv830500 | Chr.5:137672066 - 137845314 on Build GRCh38 | Loss |
|
| nsv819360 | Chr.5:137752468 - 137752870 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs79793027] 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: |
|

Genomic Map