Product Details
- SNP ID
-
hCV171852237
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:31270081 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGATGGGGATGGTGGGCTGGGAAGA[C/T]GGCTCTGGGAAAGGAGGAGAAGGTG
- Phenotype
-
MIM: 142840
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
HLA-C
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs9264621] are located under a probe and SNP(s) [rs35424484] are located under a primer 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.
Gene Details
- Gene
- HLA-C
- Gene Name
- major histocompatibility complex, class I, C
There are no transcripts associated with this gene.
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