Canonical Allele Identifier: CA358515405

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490887A>T (hg19) ; chr4:g.154569735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569735A>T , CM000666.2:g.154569735A>T	GRCh38
NC_000004.11:g.155490887A>T , CM000666.1:g.155490887A>T	GRCh37
NC_000004.10:g.155710337A>T	NCBI36
NG_008833.1:g.11756A>T , LRG_558:g.11756A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1180A>T MANE Select	ENSP00000306099.4:p.Asn394Tyr
ENST00000302068.8:c.1180A>T	ENSP00000306099.4:p.Asn394Tyr
ENST00000502545.5:n.939+428A>T
ENST00000509493.1:c.523A>T	ENSP00000426757.1:p.Asn175Tyr
NM_001184741.1:c.1003A>T	NP_001171670.1:p.Asn335Tyr
NM_005141.4:c.1180A>T , LRG_558t1:c.1180A>T	NP_005132.2:p.Asn394Tyr
NM_001382759.1:c.1048A>T	NP_001369688.1:p.Asn350Tyr
NM_001382760.1:c.1180A>T	NP_001369689.1:p.Asn394Tyr
NM_001382761.1:c.1180A>T	NP_001369690.1:p.Asn394Tyr
NM_001382762.1:c.880A>T	NP_001369691.1:p.Asn294Tyr
NM_001382763.1:c.1171A>T	NP_001369692.1:p.Asn391Tyr
NM_001382764.1:c.1081-38A>T	NP_001369693.1:n.1081-38A>T
NM_001382765.1:c.1180A>T	NP_001369694.1:p.Asn394Tyr
NM_005141.5:c.1180A>T MANE Select	NP_005132.2:p.Asn394Tyr