Canonical Allele Identifier: CA3114464
Gene: FGB HGNC NCBI

Linked Data

dbSNP Id: rs765345762

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565859G>T , CM000666.2:g.154565859G>T GRCh38
NC_000004.11:g.155487011G>T , CM000666.1:g.155487011G>T GRCh37
NC_000004.10:g.155706461G>T NCBI36
NG_008833.1:g.7880G>T , LRG_558:g.7880G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.166G>T MANE Select ENSP00000306099.4:p.Ala56Ser
ENST00000302068.8:c.166G>T ENSP00000306099.4:p.Ala56Ser
ENST00000425838.5:c.*78G>T ENSP00000398719.1:n.*78G>T
ENST00000473984.1:n.79G>T
ENST00000497097.5:n.173G>T
ENST00000498375.2:n.796G>T
ENST00000502545.5:n.147G>T
ENST00000509493.1:c.-167-1734G>T ENSP00000426757.1:n.-167-1734G>T
NM_001184741.1:c.165+1G>T NP_001171670.1:n.165+1G>T
NM_005141.4:c.166G>T , LRG_558t1:c.166G>T NP_005132.2:p.Ala56Ser
NM_001382759.1:c.166G>T NP_001369688.1:p.Ala56Ser
NM_001382760.1:c.166G>T NP_001369689.1:p.Ala56Ser
NM_001382761.1:c.166G>T NP_001369690.1:p.Ala56Ser
NM_001382762.1:c.166G>T NP_001369691.1:p.Ala56Ser
NM_001382763.1:c.166G>T NP_001369692.1:p.Ala56Ser
NM_001382764.1:c.166G>T NP_001369693.1:p.Ala56Ser
NM_001382765.1:c.166G>T NP_001369694.1:p.Ala56Ser
NM_005141.5:c.166G>T MANE Select NP_005132.2:p.Ala56Ser