Canonical Allele Identifier: CA1504935653

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569790A= , CM000666.2:g.154569790A=	GRCh38
NC_000004.11:g.155490942A= , CM000666.1:g.155490942A=	GRCh37
NC_000004.10:g.155710392A=	NCBI36
NG_008833.1:g.11811A= , LRG_558:g.11811A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1235A= MANE Select	ENSP00000306099.4:p.Asn412=
ENST00000302068.8:c.1235A=	ENSP00000306099.4:p.Asn412=
ENST00000502545.5:n.939+483A=
ENST00000509493.1:c.578A=	ENSP00000426757.1:p.Asn193=
NM_001184741.1:c.1058A=	NP_001171670.1:p.Asn353=
NM_005141.4:c.1235A= , LRG_558t1:c.1235A=	NP_005132.2:p.Asn412=
NM_001382759.1:c.1103A=	NP_001369688.1:p.Asn368=
NM_001382760.1:c.1235A=	NP_001369689.1:p.Asn412=
NM_001382761.1:c.1235A=	NP_001369690.1:p.Asn412=
NM_001382762.1:c.935A=	NP_001369691.1:p.Asn312=
NM_001382763.1:c.1226A=	NP_001369692.1:p.Asn409=
NM_001382764.1:c.*9A=	NP_001369693.1:n.*9A=
NM_001382765.1:c.1220+15A=	NP_001369694.1:n.1220+15A=
NM_005141.5:c.1235A= MANE Select	NP_005132.2:p.Asn412=