Product Details

SNP ID

rs6053

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:154563022 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGATCTCTCAGTTAAGTCTACATG[A/G]AAAGGATGGTTTCTTGGAGCTTCCA

Phenotype

MIM: 134830

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FGB PubMed Links

Gene Details

Gene

FGB

Gene Name

fibrinogen beta chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184741.1	43	Missense Mutation	AAA,GAA	K2E	NP_001171670.1
NM_005141.4	43	Missense Mutation	AAA,GAA	K2E	NP_005132.2

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