Canonical Allele Identifier: CA358514935

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490761G>A (hg19) ; chr4:g.154569609G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569609G>A , CM000666.2:g.154569609G>A	GRCh38
NC_000004.11:g.155490761G>A , CM000666.1:g.155490761G>A	GRCh37
NC_000004.10:g.155710211G>A	NCBI36
NG_008833.1:g.11630G>A , LRG_558:g.11630G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1054G>A MANE Select	ENSP00000306099.4:p.Val352Ile
ENST00000302068.8:c.1054G>A	ENSP00000306099.4:p.Val352Ile
ENST00000502545.5:n.939+302G>A
ENST00000509493.1:c.397G>A	ENSP00000426757.1:p.Val133Ile
NM_001184741.1:c.877G>A	NP_001171670.1:p.Val293Ile
NM_005141.4:c.1054G>A , LRG_558t1:c.1054G>A	NP_005132.2:p.Val352Ile
NM_001382759.1:c.922G>A	NP_001369688.1:p.Val308Ile
NM_001382760.1:c.1054G>A	NP_001369689.1:p.Val352Ile
NM_001382761.1:c.1054G>A	NP_001369690.1:p.Val352Ile
NM_001382762.1:c.754G>A	NP_001369691.1:p.Val252Ile
NM_001382763.1:c.1045G>A	NP_001369692.1:p.Val349Ile
NM_001382764.1:c.1054G>A	NP_001369693.1:p.Val352Ile
NM_001382765.1:c.1054G>A	NP_001369694.1:p.Val352Ile
NM_005141.5:c.1054G>A MANE Select	NP_005132.2:p.Val352Ile