Canonical Allele Identifier: CA358515053

Gene: FGB

Linked Data

• dbSNP Id: rs1253553035
• gnomAD v2: 4-155490792-A-G
• gnomAD v4: 4-154569640-A-G
• MyVariant Identifiers: chr4:g.155490792A>G (hg19) ; chr4:g.154569640A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569640A>G , CM000666.2:g.154569640A>G	GRCh38
NC_000004.11:g.155490792A>G , CM000666.1:g.155490792A>G	GRCh37
NC_000004.10:g.155710242A>G	NCBI36
NG_008833.1:g.11661A>G , LRG_558:g.11661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1085A>G MANE Select	ENSP00000306099.4:p.Gln362Arg
ENST00000302068.8:c.1085A>G	ENSP00000306099.4:p.Gln362Arg
ENST00000502545.5:n.939+333A>G
ENST00000509493.1:c.428A>G	ENSP00000426757.1:p.Gln143Arg
NM_001184741.1:c.908A>G	NP_001171670.1:p.Gln303Arg
NM_005141.4:c.1085A>G , LRG_558t1:c.1085A>G	NP_005132.2:p.Gln362Arg
NM_001382759.1:c.953A>G	NP_001369688.1:p.Gln318Arg
NM_001382760.1:c.1085A>G	NP_001369689.1:p.Gln362Arg
NM_001382761.1:c.1085A>G	NP_001369690.1:p.Gln362Arg
NM_001382762.1:c.785A>G	NP_001369691.1:p.Gln262Arg
NM_001382763.1:c.1076A>G	NP_001369692.1:p.Gln359Arg
NM_001382764.1:c.1080+5A>G	NP_001369693.1:n.1080+5A>G
NM_001382765.1:c.1085A>G	NP_001369694.1:p.Gln362Arg
NM_005141.5:c.1085A>G MANE Select	NP_005132.2:p.Gln362Arg