Product Details
- Assay Reference Genome
Location
Chr.12:13542369 on build GRCh38
- Cytoband
- 12p13.1
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs73290077] 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.
Target Gene Details
- Entrez Gene ID
- 2904
- Gene Symbol
- GRIN2B
- Gene Name
- glutamate ionotropic receptor NMDA type subunit 2B
- Gene Aliases
- EIEE27, GluN2B, MRD6, NMDAR2B, NR2B, hNR3
- Location
- Chr.12:13537337-13982012 on build GRCh38
- Assay Gene Location
- Within Exon 16
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