Canonical Allele Identifier: CA1504935641

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569779T= , CM000666.2:g.154569779T=	GRCh38
NC_000004.11:g.155490931T= , CM000666.1:g.155490931T=	GRCh37
NC_000004.10:g.155710381T=	NCBI36
NG_008833.1:g.11800T= , LRG_558:g.11800T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1224T= MANE Select	ENSP00000306099.4:p.Tyr408=
ENST00000302068.8:c.1224T=	ENSP00000306099.4:p.Tyr408=
ENST00000502545.5:n.939+472T=
ENST00000509493.1:c.567T=	ENSP00000426757.1:p.Tyr189=
NM_001184741.1:c.1047T=	NP_001171670.1:p.Tyr349=
NM_005141.4:c.1224T= , LRG_558t1:c.1224T=	NP_005132.2:p.Tyr408=
NM_001382759.1:c.1092T=	NP_001369688.1:p.Tyr364=
NM_001382760.1:c.1224T=	NP_001369689.1:p.Tyr408=
NM_001382761.1:c.1224T=	NP_001369690.1:p.Tyr408=
NM_001382762.1:c.924T=	NP_001369691.1:p.Tyr308=
NM_001382763.1:c.1215T=	NP_001369692.1:p.Tyr405=
NM_001382764.1:c.1087T=	NP_001369693.1:p.Ter363=
NM_001382765.1:c.1220+4T=	NP_001369694.1:n.1220+4T=
NM_005141.5:c.1224T= MANE Select	NP_005132.2:p.Tyr408=