Canonical Allele Identifier: CA108751733

Gene: FGB

Linked Data

• dbSNP Id: rs1012680020
• MyVariant Identifiers: chr4:g.155490903T>C (hg19) ; chr4:g.154569751T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569751T>C , CM000666.2:g.154569751T>C	GRCh38
NC_000004.11:g.155490903T>C , CM000666.1:g.155490903T>C	GRCh37
NC_000004.10:g.155710353T>C	NCBI36
NG_008833.1:g.11772T>C , LRG_558:g.11772T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1196T>C MANE Select	ENSP00000306099.4:p.Ile399Thr
ENST00000302068.8:c.1196T>C	ENSP00000306099.4:p.Ile399Thr
ENST00000502545.5:n.939+444T>C
ENST00000509493.1:c.539T>C	ENSP00000426757.1:p.Ile180Thr
NM_001184741.1:c.1019T>C	NP_001171670.1:p.Ile340Thr
NM_005141.4:c.1196T>C , LRG_558t1:c.1196T>C	NP_005132.2:p.Ile399Thr
NM_001382759.1:c.1064T>C	NP_001369688.1:p.Ile355Thr
NM_001382760.1:c.1196T>C	NP_001369689.1:p.Ile399Thr
NM_001382761.1:c.1196T>C	NP_001369690.1:p.Ile399Thr
NM_001382762.1:c.896T>C	NP_001369691.1:p.Ile299Thr
NM_001382763.1:c.1187T>C	NP_001369692.1:p.Ile396Thr
NM_001382764.1:c.1081-22T>C	NP_001369693.1:n.1081-22T>C
NM_001382765.1:c.1196T>C	NP_001369694.1:p.Ile399Thr
NM_005141.5:c.1196T>C MANE Select	NP_005132.2:p.Ile399Thr