Canonical Allele Identifier: CA358515375

Gene: FGB

Linked Data

• dbSNP Id: rs1730337451
• gnomAD v3: 4-154569728-G-A
• gnomAD v4: 4-154569728-G-A
• MyVariant Identifiers: chr4:g.155490880G>A (hg19) ; chr4:g.154569728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569728G>A , CM000666.2:g.154569728G>A	GRCh38
NC_000004.11:g.155490880G>A , CM000666.1:g.155490880G>A	GRCh37
NC_000004.10:g.155710330G>A	NCBI36
NG_008833.1:g.11749G>A , LRG_558:g.11749G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1173G>A MANE Select	ENSP00000306099.4:p.Met391Ile
ENST00000302068.8:c.1173G>A	ENSP00000306099.4:p.Met391Ile
ENST00000502545.5:n.939+421G>A
ENST00000509493.1:c.516G>A	ENSP00000426757.1:p.Met172Ile
NM_001184741.1:c.996G>A	NP_001171670.1:p.Met332Ile
NM_005141.4:c.1173G>A , LRG_558t1:c.1173G>A	NP_005132.2:p.Met391Ile
NM_001382759.1:c.1041G>A	NP_001369688.1:p.Met347Ile
NM_001382760.1:c.1173G>A	NP_001369689.1:p.Met391Ile
NM_001382761.1:c.1173G>A	NP_001369690.1:p.Met391Ile
NM_001382762.1:c.873G>A	NP_001369691.1:p.Met291Ile
NM_001382763.1:c.1164G>A	NP_001369692.1:p.Met388Ile
NM_001382764.1:c.1081-45G>A	NP_001369693.1:n.1081-45G>A
NM_001382765.1:c.1173G>A	NP_001369694.1:p.Met391Ile
NM_005141.5:c.1173G>A MANE Select	NP_005132.2:p.Met391Ile