Canonical Allele Identifier: CA358515341

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490870C>A (hg19) ; chr4:g.154569718C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569718C>A , CM000666.2:g.154569718C>A	GRCh38
NC_000004.11:g.155490870C>A , CM000666.1:g.155490870C>A	GRCh37
NC_000004.10:g.155710320C>A	NCBI36
NG_008833.1:g.11739C>A , LRG_558:g.11739C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1163C>A MANE Select	ENSP00000306099.4:p.Ser388Tyr
ENST00000302068.8:c.1163C>A	ENSP00000306099.4:p.Ser388Tyr
ENST00000502545.5:n.939+411C>A
ENST00000509493.1:c.506C>A	ENSP00000426757.1:p.Ser169Tyr
NM_001184741.1:c.986C>A	NP_001171670.1:p.Ser329Tyr
NM_005141.4:c.1163C>A , LRG_558t1:c.1163C>A	NP_005132.2:p.Ser388Tyr
NM_001382759.1:c.1031C>A	NP_001369688.1:p.Ser344Tyr
NM_001382760.1:c.1163C>A	NP_001369689.1:p.Ser388Tyr
NM_001382761.1:c.1163C>A	NP_001369690.1:p.Ser388Tyr
NM_001382762.1:c.863C>A	NP_001369691.1:p.Ser288Tyr
NM_001382763.1:c.1154C>A	NP_001369692.1:p.Ser385Tyr
NM_001382764.1:c.1081-55C>A	NP_001369693.1:n.1081-55C>A
NM_001382765.1:c.1163C>A	NP_001369694.1:p.Ser388Tyr
NM_005141.5:c.1163C>A MANE Select	NP_005132.2:p.Ser388Tyr