Canonical Allele Identifier: CA1504935470

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569680C= , CM000666.2:g.154569680C=	GRCh38
NC_000004.11:g.155490832C= , CM000666.1:g.155490832C=	GRCh37
NC_000004.10:g.155710282C=	NCBI36
NG_008833.1:g.11701C= , LRG_558:g.11701C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1125C= MANE Select	ENSP00000306099.4:p.Tyr375=
ENST00000302068.8:c.1125C=	ENSP00000306099.4:p.Tyr375=
ENST00000502545.5:n.939+373C=
ENST00000509493.1:c.468C=	ENSP00000426757.1:p.Tyr156=
NM_001184741.1:c.948C=	NP_001171670.1:p.Tyr316=
NM_005141.4:c.1125C= , LRG_558t1:c.1125C=	NP_005132.2:p.Tyr375=
NM_001382759.1:c.993C=	NP_001369688.1:p.Tyr331=
NM_001382760.1:c.1125C=	NP_001369689.1:p.Tyr375=
NM_001382761.1:c.1125C=	NP_001369690.1:p.Tyr375=
NM_001382762.1:c.825C=	NP_001369691.1:p.Tyr275=
NM_001382763.1:c.1116C=	NP_001369692.1:p.Tyr372=
NM_001382764.1:c.1080+45C=	NP_001369693.1:n.1080+45C=
NM_001382765.1:c.1125C=	NP_001369694.1:p.Tyr375=
NM_005141.5:c.1125C= MANE Select	NP_005132.2:p.Tyr375=