Canonical Allele Identifier: CA358508420
Gene: FGB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154565867C>A , CM000666.2:g.154565867C>A GRCh38
NC_000004.11:g.155487019C>A , CM000666.1:g.155487019C>A GRCh37
NC_000004.10:g.155706469C>A NCBI36
NG_008833.1:g.7888C>A , LRG_558:g.7888C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.174C>A MANE Select ENSP00000306099.4:p.Ser58Arg
ENST00000302068.8:c.174C>A ENSP00000306099.4:p.Ser58Arg
ENST00000425838.5:c.*86C>A ENSP00000398719.1:n.*86C>A
ENST00000473984.1:n.87C>A
ENST00000497097.5:n.181C>A
ENST00000498375.2:n.804C>A
ENST00000502545.5:n.155C>A
ENST00000509493.1:c.-167-1726C>A ENSP00000426757.1:n.-167-1726C>A
NM_001184741.1:c.165+9C>A NP_001171670.1:n.165+9C>A
NM_005141.4:c.174C>A , LRG_558t1:c.174C>A NP_005132.2:p.Ser58Arg
NM_001382759.1:c.174C>A NP_001369688.1:p.Ser58Arg
NM_001382760.1:c.174C>A NP_001369689.1:p.Ser58Arg
NM_001382761.1:c.174C>A NP_001369690.1:p.Ser58Arg
NM_001382762.1:c.174C>A NP_001369691.1:p.Ser58Arg
NM_001382763.1:c.174C>A NP_001369692.1:p.Ser58Arg
NM_001382764.1:c.174C>A NP_001369693.1:p.Ser58Arg
NM_001382765.1:c.174C>A NP_001369694.1:p.Ser58Arg
NM_005141.5:c.174C>A MANE Select NP_005132.2:p.Ser58Arg