Canonical Allele Identifier: CA1504935389

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569640A= , CM000666.2:g.154569640A=	GRCh38
NC_000004.11:g.155490792A= , CM000666.1:g.155490792A=	GRCh37
NC_000004.10:g.155710242A=	NCBI36
NG_008833.1:g.11661A= , LRG_558:g.11661A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1085A= MANE Select	ENSP00000306099.4:p.Gln362=
ENST00000302068.8:c.1085A=	ENSP00000306099.4:p.Gln362=
ENST00000502545.5:n.939+333A=
ENST00000509493.1:c.428A=	ENSP00000426757.1:p.Gln143=
NM_001184741.1:c.908A=	NP_001171670.1:p.Gln303=
NM_005141.4:c.1085A= , LRG_558t1:c.1085A=	NP_005132.2:p.Gln362=
NM_001382759.1:c.953A=	NP_001369688.1:p.Gln318=
NM_001382760.1:c.1085A=	NP_001369689.1:p.Gln362=
NM_001382761.1:c.1085A=	NP_001369690.1:p.Gln362=
NM_001382762.1:c.785A=	NP_001369691.1:p.Gln262=
NM_001382763.1:c.1076A=	NP_001369692.1:p.Gln359=
NM_001382764.1:c.1080+5A=	NP_001369693.1:n.1080+5A=
NM_001382765.1:c.1085A=	NP_001369694.1:p.Gln362=
NM_005141.5:c.1085A= MANE Select	NP_005132.2:p.Gln362=