Product Details

SNP ID
rs9267673
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:31915902 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGAGCCTCAATGGCTGCCTCAACT[C/T]GGTGTAGCGCTGACTGGCTCACATA
Phenotype
MIM: 613927
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C2 PubMed Links

Gene Details

Gene
C2
Gene Name
complement component 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000063.5 Intron NP_000054.2
NM_001145903.2 Intron NP_001139375.1
NM_001178063.2 Intron NP_001171534.1
NM_001282457.1 Intron NP_001269386.1
NM_001282458.1 Intron NP_001269387.1
NM_001282459.1 Intron NP_001269388.1

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