ClinVar

NM_005141.5(FGB):c.115-579C>T

Gene:

FGB:fibrinogen beta chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q31.3

Genomic location:

• Chr4: 154565229 (on Assembly GRCh38)
• Chr4: 155486381 (on Assembly GRCh37)

Preferred name:

NM_005141.5(FGB):c.115-579C>T

HGVS:

• NC_000004.12:g.154565229C>T
• NG_008833.1:g.7250C>T
• NM_001184741.1:c.115-579C>T
• NM_001382759.1:c.115-579C>T
• NM_001382760.1:c.115-579C>T
• NM_001382761.1:c.115-579C>T
• NM_001382762.1:c.115-579C>T
• NM_001382763.1:c.115-579C>T
• NM_001382764.1:c.115-579C>T
• NM_001382765.1:c.115-579C>T
• NM_005141.5:c.115-579C>TMANE SELECT
• LRG_558:g.7250C>T
• NC_000004.11:g.155486381C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs2227401

NCBI 1000 Genomes Browser:

rs2227401

Molecular consequence:

• NM_001184741.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382759.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382760.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382761.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382762.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382763.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382764.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001382765.1:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_005141.5:c.115-579C>T - intron variant - [Sequence Ontology: SO:0001627]