Product Details

SNP ID

rs12734951

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:197042524 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAAAAATGTATTCAGGTGAGTTC[A/C]ACATCTATGTGAGGCTGGGCGTGGT

Phenotype

MIM: 134580

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

F13B PubMed Links

Gene Details

Gene

F13B

Gene Name

coagulation factor XIII B chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001994.2		Intron			NP_001985.2
XM_011509283.2		Intron			XP_011507585.1
XM_011509284.2		Intron			XP_011507586.1
XM_011509286.2		Intron			XP_011507588.1

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