Canonical Allele Identifier: CA1504935425

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569662G= , CM000666.2:g.154569662G=	GRCh38
NC_000004.11:g.155490814G= , CM000666.1:g.155490814G=	GRCh37
NC_000004.10:g.155710264G=	NCBI36
NG_008833.1:g.11683G= , LRG_558:g.11683G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1107G= MANE Select	ENSP00000306099.4:p.Gln369=
ENST00000302068.8:c.1107G=	ENSP00000306099.4:p.Gln369=
ENST00000502545.5:n.939+355G=
ENST00000509493.1:c.450G=	ENSP00000426757.1:p.Gln150=
NM_001184741.1:c.930G=	NP_001171670.1:p.Gln310=
NM_005141.4:c.1107G= , LRG_558t1:c.1107G=	NP_005132.2:p.Gln369=
NM_001382759.1:c.975G=	NP_001369688.1:p.Gln325=
NM_001382760.1:c.1107G=	NP_001369689.1:p.Gln369=
NM_001382761.1:c.1107G=	NP_001369690.1:p.Gln369=
NM_001382762.1:c.807G=	NP_001369691.1:p.Gln269=
NM_001382763.1:c.1098G=	NP_001369692.1:p.Gln366=
NM_001382764.1:c.1080+27G=	NP_001369693.1:n.1080+27G=
NM_001382765.1:c.1107G=	NP_001369694.1:p.Gln369=
NM_005141.5:c.1107G= MANE Select	NP_005132.2:p.Gln369=