Canonical Allele Identifier: CA108751572

Gene: FGB

Linked Data

• dbSNP Id: rs751610009
• MyVariant Identifiers: chr4:g.155490733A>T (hg19) ; chr4:g.154569581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569581A>T , CM000666.2:g.154569581A>T	GRCh38
NC_000004.11:g.155490733A>T , CM000666.1:g.155490733A>T	GRCh37
NC_000004.10:g.155710183A>T	NCBI36
NG_008833.1:g.11602A>T , LRG_558:g.11602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1026A>T MANE Select	ENSP00000306099.4:p.Ile342=
ENST00000302068.8:c.1026A>T	ENSP00000306099.4:p.Ile342=
ENST00000502545.5:n.939+274A>T
ENST00000509493.1:c.369A>T	ENSP00000426757.1:p.Ile123=
NM_001184741.1:c.849A>T	NP_001171670.1:p.Ile283=
NM_005141.4:c.1026A>T , LRG_558t1:c.1026A>T	NP_005132.2:p.Ile342=
NM_001382759.1:c.894A>T	NP_001369688.1:p.Ile298=
NM_001382760.1:c.1026A>T	NP_001369689.1:p.Ile342=
NM_001382761.1:c.1026A>T	NP_001369690.1:p.Ile342=
NM_001382762.1:c.746-20A>T	NP_001369691.1:n.746-20A>T
NM_001382763.1:c.1017A>T	NP_001369692.1:p.Ile339=
NM_001382764.1:c.1026A>T	NP_001369693.1:p.Ile342=
NM_001382765.1:c.1026A>T	NP_001369694.1:p.Ile342=
NM_005141.5:c.1026A>T MANE Select	NP_005132.2:p.Ile342=