Canonical Allele Identifier: CA1504935628

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569762A= , CM000666.2:g.154569762A=	GRCh38
NC_000004.11:g.155490914A= , CM000666.1:g.155490914A=	GRCh37
NC_000004.10:g.155710364A=	NCBI36
NG_008833.1:g.11783A= , LRG_558:g.11783A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1207A= MANE Select	ENSP00000306099.4:p.Met403=
ENST00000302068.8:c.1207A=	ENSP00000306099.4:p.Met403=
ENST00000502545.5:n.939+455A=
ENST00000509493.1:c.550A=	ENSP00000426757.1:p.Met184=
NM_001184741.1:c.1030A=	NP_001171670.1:p.Met344=
NM_005141.4:c.1207A= , LRG_558t1:c.1207A=	NP_005132.2:p.Met403=
NM_001382759.1:c.1075A=	NP_001369688.1:p.Met359=
NM_001382760.1:c.1207A=	NP_001369689.1:p.Met403=
NM_001382761.1:c.1207A=	NP_001369690.1:p.Met403=
NM_001382762.1:c.907A=	NP_001369691.1:p.Met303=
NM_001382763.1:c.1198A=	NP_001369692.1:p.Met400=
NM_001382764.1:c.1081-11A=	NP_001369693.1:n.1081-11A=
NM_001382765.1:c.1207A=	NP_001369694.1:p.Met403=
NM_005141.5:c.1207A= MANE Select	NP_005132.2:p.Met403=