Genomic Map
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Target Gene Details
Entrez Gene ID: | 7137 |
Gene Name: | troponin I3, cardiac type |
Gene Aliases: |
CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI |
Location: |
Chr.19:55151767-55157732 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TNNI3 | NM_000363.4 | NP_000354.4 | ||
| AK223451.1 | BAD97171.1 | |||
| BC096165.1 | AAH96165.1 | |||
| BC096166.1 | AAH96166.1 | |||
| BC096167.3 | AAH96167.1 | |||
| BC099631.3 | AAH99631.1 | |||
| BT019517.1 | AAV38324.1 | |||
| CR541985.1 | CAG46782.1 | |||
| CR542012.1 | CAG46809.1 | |||
| EU747720.1 | ||||
| M64247.1 | AAA16157.1 | |||
| X54163.1 | CAA38102.1 |
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Additional Information:
For this assay, SNP(s) [rs73617692] 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: |
Intragenic
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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