Product Details

SNP ID
rs2858993
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:26087628 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAACTTTGGAGGACCTGCTCAACCC[A/T]ATCCGCAAGCCCCTCTCCCTACTTT
Phenotype
MIM: 613609
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
HFE PubMed Links

Gene Details

Gene
HFE
Gene Name
hemochromatosis
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000410.3 Intron NP_000401.1
NM_001300749.1 Intron NP_001287678.1
NM_139003.2 Intron NP_620572.1
NM_139004.2 Intron NP_620573.1
NM_139006.2 Intron NP_620575.1
NM_139007.2 Intron NP_620576.1
NM_139008.2 Intron NP_620577.1
NM_139009.2 Intron NP_620578.1
NM_139010.2 Intron NP_620579.1
NM_139011.2 Intron NP_620580.1
XM_011514543.2 Intron XP_011512845.1

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