Canonical Allele Identifier: CA358515042

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490789T>A (hg19) ; chr4:g.154569637T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569637T>A , CM000666.2:g.154569637T>A	GRCh38
NC_000004.11:g.155490789T>A , CM000666.1:g.155490789T>A	GRCh37
NC_000004.10:g.155710239T>A	NCBI36
NG_008833.1:g.11658T>A , LRG_558:g.11658T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1082T>A MANE Select	ENSP00000306099.4:p.Val361Glu
ENST00000302068.8:c.1082T>A	ENSP00000306099.4:p.Val361Glu
ENST00000502545.5:n.939+330T>A
ENST00000509493.1:c.425T>A	ENSP00000426757.1:p.Val142Glu
NM_001184741.1:c.905T>A	NP_001171670.1:p.Val302Glu
NM_005141.4:c.1082T>A , LRG_558t1:c.1082T>A	NP_005132.2:p.Val361Glu
NM_001382759.1:c.950T>A	NP_001369688.1:p.Val317Glu
NM_001382760.1:c.1082T>A	NP_001369689.1:p.Val361Glu
NM_001382761.1:c.1082T>A	NP_001369690.1:p.Val361Glu
NM_001382762.1:c.782T>A	NP_001369691.1:p.Val261Glu
NM_001382763.1:c.1073T>A	NP_001369692.1:p.Val358Glu
NM_001382764.1:c.1080+2T>A	NP_001369693.1:n.1080+2T>A
NM_001382765.1:c.1082T>A	NP_001369694.1:p.Val361Glu
NM_005141.5:c.1082T>A MANE Select	NP_005132.2:p.Val361Glu