Canonical Allele Identifier: CA358515590

Gene: FGB

Linked Data

• gnomAD v4: 4-154569781-A-T
• MyVariant Identifiers: chr4:g.155490933A>T (hg19) ; chr4:g.154569781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569781A>T , CM000666.2:g.154569781A>T	GRCh38
NC_000004.11:g.155490933A>T , CM000666.1:g.155490933A>T	GRCh37
NC_000004.10:g.155710383A>T	NCBI36
NG_008833.1:g.11802A>T , LRG_558:g.11802A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1226A>T MANE Select	ENSP00000306099.4:p.Asp409Val
ENST00000302068.8:c.1226A>T	ENSP00000306099.4:p.Asp409Val
ENST00000502545.5:n.939+474A>T
ENST00000509493.1:c.569A>T	ENSP00000426757.1:p.Asp190Val
NM_001184741.1:c.1049A>T	NP_001171670.1:p.Asp350Val
NM_005141.4:c.1226A>T , LRG_558t1:c.1226A>T	NP_005132.2:p.Asp409Val
NM_001382759.1:c.1094A>T	NP_001369688.1:p.Asp365Val
NM_001382760.1:c.1226A>T	NP_001369689.1:p.Asp409Val
NM_001382761.1:c.1226A>T	NP_001369690.1:p.Asp409Val
NM_001382762.1:c.926A>T	NP_001369691.1:p.Asp309Val
NM_001382763.1:c.1217A>T	NP_001369692.1:p.Asp406Val
NM_001382764.1:c.1089A>T	NP_001369693.1:p.Ter363Cys
NM_001382765.1:c.1220+6A>T	NP_001369694.1:n.1220+6A>T
NM_005141.5:c.1226A>T MANE Select	NP_005132.2:p.Asp409Val