Canonical Allele Identifier: CA358515370

Gene: FGB

Linked Data

• dbSNP Id: rs1578785473
• gnomAD v4: 4-154569726-A-G
• MyVariant Identifiers: chr4:g.155490878A>G (hg19) ; chr4:g.154569726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569726A>G , CM000666.2:g.154569726A>G	GRCh38
NC_000004.11:g.155490878A>G , CM000666.1:g.155490878A>G	GRCh37
NC_000004.10:g.155710328A>G	NCBI36
NG_008833.1:g.11747A>G , LRG_558:g.11747A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1171A>G MANE Select	ENSP00000306099.4:p.Met391Val
ENST00000302068.8:c.1171A>G	ENSP00000306099.4:p.Met391Val
ENST00000502545.5:n.939+419A>G
ENST00000509493.1:c.514A>G	ENSP00000426757.1:p.Met172Val
NM_001184741.1:c.994A>G	NP_001171670.1:p.Met332Val
NM_005141.4:c.1171A>G , LRG_558t1:c.1171A>G	NP_005132.2:p.Met391Val
NM_001382759.1:c.1039A>G	NP_001369688.1:p.Met347Val
NM_001382760.1:c.1171A>G	NP_001369689.1:p.Met391Val
NM_001382761.1:c.1171A>G	NP_001369690.1:p.Met391Val
NM_001382762.1:c.871A>G	NP_001369691.1:p.Met291Val
NM_001382763.1:c.1162A>G	NP_001369692.1:p.Met388Val
NM_001382764.1:c.1081-47A>G	NP_001369693.1:n.1081-47A>G
NM_001382765.1:c.1171A>G	NP_001369694.1:p.Met391Val
NM_005141.5:c.1171A>G MANE Select	NP_005132.2:p.Met391Val