FGB fibrinogen beta chain

Information
Symbol
FGB
Type
protein-coding
Description
fibrinogen beta chain
Entrez Gene ID
2244
Genome
hg19
Position
chr4:155,484,163-155,493,959
Genome
hg38
Position
chr4:154,563,011-154,572,807
MIM
134830 OMIM
HGNC
HGNC:3662 HGNC
Ensembl
ENSG00000171564 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 12
Benign 0 80
Likely benign 0 44
Conflicting classifications of pathogenicity 0 16
other 0 8
Uncertain significance 0 202
Ranking
ClinVar
0
0
44
292
22
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM HEL-S-78p
MIM 134830 OMIM
HGNC HGNC:3662 HGNC
Ensembl ENSG00000171564 Ensembl
AllianceGenome HGNC:3662
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302068.9 hg38 chr4 154,563,011 154,572,807 9,797
ENST00000509493.1 hg38 chr4 154,563,026 154,570,721 7,696
ENST00000302068.9 hg19 chr4 155,484,163 155,493,959 9,797
ENST00000509493.1 hg19 chr4 155,484,178 155,491,873 7,696
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