Canonical Allele Identifier: CA358515426

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490893A>G (hg19) ; chr4:g.154569741A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569741A>G , CM000666.2:g.154569741A>G	GRCh38
NC_000004.11:g.155490893A>G , CM000666.1:g.155490893A>G	GRCh37
NC_000004.10:g.155710343A>G	NCBI36
NG_008833.1:g.11762A>G , LRG_558:g.11762A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1186A>G MANE Select	ENSP00000306099.4:p.Thr396Ala
ENST00000302068.8:c.1186A>G	ENSP00000306099.4:p.Thr396Ala
ENST00000502545.5:n.939+434A>G
ENST00000509493.1:c.529A>G	ENSP00000426757.1:p.Thr177Ala
NM_001184741.1:c.1009A>G	NP_001171670.1:p.Thr337Ala
NM_005141.4:c.1186A>G , LRG_558t1:c.1186A>G	NP_005132.2:p.Thr396Ala
NM_001382759.1:c.1054A>G	NP_001369688.1:p.Thr352Ala
NM_001382760.1:c.1186A>G	NP_001369689.1:p.Thr396Ala
NM_001382761.1:c.1186A>G	NP_001369690.1:p.Thr396Ala
NM_001382762.1:c.886A>G	NP_001369691.1:p.Thr296Ala
NM_001382763.1:c.1177A>G	NP_001369692.1:p.Thr393Ala
NM_001382764.1:c.1081-32A>G	NP_001369693.1:n.1081-32A>G
NM_001382765.1:c.1186A>G	NP_001369694.1:p.Thr396Ala
NM_005141.5:c.1186A>G MANE Select	NP_005132.2:p.Thr396Ala