Product Details

SNP ID

rs185920746

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:154584674 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAGTCTTGCCAGGTCCGGTTAAAA[G/T]TCAGTGATCCATCCATTCTTTGCTG

Phenotype

MIM: 134820

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FGA PubMed Links

Gene Details

Gene

FGA

Gene Name

fibrinogen alpha chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000508.4	2130	Missense Mutation			NP_000499.1
NM_021871.3	2130	Intron			NP_068657.1

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