Canonical Allele Identifier: CA3114741
Gene: FGB HGNC NCBI

Linked Data

dbSNP Id: rs200792588

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154569759G>A , CM000666.2:g.154569759G>A GRCh38
NC_000004.11:g.155490911G>A , CM000666.1:g.155490911G>A GRCh37
NC_000004.10:g.155710361G>A NCBI36
NG_008833.1:g.11780G>A , LRG_558:g.11780G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302068.9:c.1204G>A MANE Select ENSP00000306099.4:p.Gly402Ser
ENST00000302068.8:c.1204G>A ENSP00000306099.4:p.Gly402Ser
ENST00000502545.5:n.939+452G>A
ENST00000509493.1:c.547G>A ENSP00000426757.1:p.Gly183Ser
NM_001184741.1:c.1027G>A NP_001171670.1:p.Gly343Ser
NM_005141.4:c.1204G>A , LRG_558t1:c.1204G>A NP_005132.2:p.Gly402Ser
NM_001382759.1:c.1072G>A NP_001369688.1:p.Gly358Ser
NM_001382760.1:c.1204G>A NP_001369689.1:p.Gly402Ser
NM_001382761.1:c.1204G>A NP_001369690.1:p.Gly402Ser
NM_001382762.1:c.904G>A NP_001369691.1:p.Gly302Ser
NM_001382763.1:c.1195G>A NP_001369692.1:p.Gly399Ser
NM_001382764.1:c.1081-14G>A NP_001369693.1:n.1081-14G>A
NM_001382765.1:c.1204G>A NP_001369694.1:p.Gly402Ser
NM_005141.5:c.1204G>A MANE Select NP_005132.2:p.Gly402Ser