Canonical Allele Identifier: CA126440
Gene: FGB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16387
ClinVar RCV Id: RCV000017811
dbSNP Id: rs121909620

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565985G>A , CM000666.2:g.154565985G>A GRCh38
NC_000004.11:g.155487137G>A , CM000666.1:g.155487137G>A GRCh37
NC_000004.10:g.155706587G>A NCBI36
NG_008833.1:g.8006G>A , LRG_558:g.8006G>A

Transcript Alleles

HGVS Amino-acid change
NM_001184741.1:c.165+127G>A VV NP_001171670.1:p.=
NM_005141.4:c.292G>A , LRG_558t1:c.292G>A NP_005132.2:p.Ala98Thr
ENST00000302068.8:c.292G>A ENSP00000306099.4:p.Ala98Thr
ENST00000425838.5:c.*204G>A ENSP00000398719.1:p.=
ENST00000473984.1:n.205G>A
ENST00000497097.5:n.299G>A
ENST00000498375.2:n.922G>A
ENST00000502545.5:n.273G>A
ENST00000509493.1:c.-167-1608G>A ENSP00000426757.1:p.=