Canonical Allele Identifier: CA1504935640

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569777T= , CM000666.2:g.154569777T=	GRCh38
NC_000004.11:g.155490929T= , CM000666.1:g.155490929T=	GRCh37
NC_000004.10:g.155710379T=	NCBI36
NG_008833.1:g.11798T= , LRG_558:g.11798T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1222T= MANE Select	ENSP00000306099.4:p.Tyr408=
ENST00000302068.8:c.1222T=	ENSP00000306099.4:p.Tyr408=
ENST00000502545.5:n.939+470T=
ENST00000509493.1:c.565T=	ENSP00000426757.1:p.Tyr189=
NM_001184741.1:c.1045T=	NP_001171670.1:p.Tyr349=
NM_005141.4:c.1222T= , LRG_558t1:c.1222T=	NP_005132.2:p.Tyr408=
NM_001382759.1:c.1090T=	NP_001369688.1:p.Tyr364=
NM_001382760.1:c.1222T=	NP_001369689.1:p.Tyr408=
NM_001382761.1:c.1222T=	NP_001369690.1:p.Tyr408=
NM_001382762.1:c.922T=	NP_001369691.1:p.Tyr308=
NM_001382763.1:c.1213T=	NP_001369692.1:p.Tyr405=
NM_001382764.1:c.1085T=	NP_001369693.1:p.Val362=
NM_001382765.1:c.1220+2T=	NP_001369694.1:n.1220+2T=
NM_005141.5:c.1222T= MANE Select	NP_005132.2:p.Tyr408=