Product Details

Assay Reference Genome
Location

Chr.11:19372703 on build GRCh38

Cytoband

11p15.1

Species

Homo sapiens

Variation Type

Copy Number

Additional Information

For this assay, SNP(s) [rs78502681] 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

89797

Gene Symbol

NAV2

Gene Name

neuron navigator 2

Gene Aliases

HELAD1, POMFIL2, RAINB1, STEERIN2, UNC53H2

Location

Chr.11:19345200-20121601 on build GRCh38

Assay Gene Location

Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
NAV2	NM_001111018.1			NP_001104488.1
	XM_011520452.2			XP_011518754.1
	XM_017018520.1			XP_016874009.1
	XM_017018522.1			XP_016874011.1
	AB063115.1			BAC00853.1

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