Product Details

SNP ID

rs1049636

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:154604818 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TCTGAAACTTTGTGGGTCAATAGAA[A/G]TTAGCAGTTAATTTTCTACAAATCA

Phenotype

MIM: 134850

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FGG PubMed Links

Gene Details

Gene

FGG

Gene Name

fibrinogen gamma chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000509.5	1519	Intron			NP_000500.2
NM_021870.2	1519	UTR 3			NP_068656.2

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