Canonical Allele Identifier: CA358515277

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490852C>A (hg19) ; chr4:g.154569700C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569700C>A , CM000666.2:g.154569700C>A	GRCh38
NC_000004.11:g.155490852C>A , CM000666.1:g.155490852C>A	GRCh37
NC_000004.10:g.155710302C>A	NCBI36
NG_008833.1:g.11721C>A , LRG_558:g.11721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1145C>A MANE Select	ENSP00000306099.4:p.Ala382Asp
ENST00000302068.8:c.1145C>A	ENSP00000306099.4:p.Ala382Asp
ENST00000502545.5:n.939+393C>A
ENST00000509493.1:c.488C>A	ENSP00000426757.1:p.Ala163Asp
NM_001184741.1:c.968C>A	NP_001171670.1:p.Ala323Asp
NM_005141.4:c.1145C>A , LRG_558t1:c.1145C>A	NP_005132.2:p.Ala382Asp
NM_001382759.1:c.1013C>A	NP_001369688.1:p.Ala338Asp
NM_001382760.1:c.1145C>A	NP_001369689.1:p.Ala382Asp
NM_001382761.1:c.1145C>A	NP_001369690.1:p.Ala382Asp
NM_001382762.1:c.845C>A	NP_001369691.1:p.Ala282Asp
NM_001382763.1:c.1136C>A	NP_001369692.1:p.Ala379Asp
NM_001382764.1:c.1080+65C>A	NP_001369693.1:n.1080+65C>A
NM_001382765.1:c.1145C>A	NP_001369694.1:p.Ala382Asp
NM_005141.5:c.1145C>A MANE Select	NP_005132.2:p.Ala382Asp