Canonical Allele Identifier: CA358515565

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490927C>G (hg19) ; chr4:g.154569775C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569775C>G , CM000666.2:g.154569775C>G	GRCh38
NC_000004.11:g.155490927C>G , CM000666.1:g.155490927C>G	GRCh37
NC_000004.10:g.155710377C>G	NCBI36
NG_008833.1:g.11796C>G , LRG_558:g.11796C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1220C>G MANE Select	ENSP00000306099.4:p.Thr407Arg
ENST00000302068.8:c.1220C>G	ENSP00000306099.4:p.Thr407Arg
ENST00000502545.5:n.939+468C>G
ENST00000509493.1:c.563C>G	ENSP00000426757.1:p.Thr188Arg
NM_001184741.1:c.1043C>G	NP_001171670.1:p.Thr348Arg
NM_005141.4:c.1220C>G , LRG_558t1:c.1220C>G	NP_005132.2:p.Thr407Arg
NM_001382759.1:c.1088C>G	NP_001369688.1:p.Thr363Arg
NM_001382760.1:c.1220C>G	NP_001369689.1:p.Thr407Arg
NM_001382761.1:c.1220C>G	NP_001369690.1:p.Thr407Arg
NM_001382762.1:c.920C>G	NP_001369691.1:p.Thr307Arg
NM_001382763.1:c.1211C>G	NP_001369692.1:p.Thr404Arg
NM_001382764.1:c.1083C>G	NP_001369693.1:p.His361Gln
NM_001382765.1:c.1220C>G	NP_001369694.1:p.Thr407Arg
NM_005141.5:c.1220C>G MANE Select	NP_005132.2:p.Thr407Arg