Canonical Allele Identifier: CA1504935631

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569765T= , CM000666.2:g.154569765T=	GRCh38
NC_000004.11:g.155490917T= , CM000666.1:g.155490917T=	GRCh37
NC_000004.10:g.155710367T=	NCBI36
NG_008833.1:g.11786T= , LRG_558:g.11786T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1210T= MANE Select	ENSP00000306099.4:p.Phe404=
ENST00000302068.8:c.1210T=	ENSP00000306099.4:p.Phe404=
ENST00000502545.5:n.939+458T=
ENST00000509493.1:c.553T=	ENSP00000426757.1:p.Phe185=
NM_001184741.1:c.1033T=	NP_001171670.1:p.Phe345=
NM_005141.4:c.1210T= , LRG_558t1:c.1210T=	NP_005132.2:p.Phe404=
NM_001382759.1:c.1078T=	NP_001369688.1:p.Phe360=
NM_001382760.1:c.1210T=	NP_001369689.1:p.Phe404=
NM_001382761.1:c.1210T=	NP_001369690.1:p.Phe404=
NM_001382762.1:c.910T=	NP_001369691.1:p.Phe304=
NM_001382763.1:c.1201T=	NP_001369692.1:p.Phe401=
NM_001382764.1:c.1081-8T=	NP_001369693.1:n.1081-8T=
NM_001382765.1:c.1210T=	NP_001369694.1:p.Phe404=
NM_005141.5:c.1210T= MANE Select	NP_005132.2:p.Phe404=