Product Details

SNP ID

rs3136433

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:46720358 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGAACTCCCCTATCCTCAAATATT[A/C]TTCTCCTTTTGGAAACAAAAGTAGG

Phenotype

MIM: 176930

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

F2 PubMed Links

Gene Details

Gene

F2

Gene Name

coagulation factor II, thrombin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000506.4		Intron			NP_000497.1
NM_001311257.1		Intron			NP_001298186.1

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