Canonical Allele Identifier: CA358515533

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490920T>G (hg19) ; chr4:g.154569768T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569768T>G , CM000666.2:g.154569768T>G	GRCh38
NC_000004.11:g.155490920T>G , CM000666.1:g.155490920T>G	GRCh37
NC_000004.10:g.155710370T>G	NCBI36
NG_008833.1:g.11789T>G , LRG_558:g.11789T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1213T>G MANE Select	ENSP00000306099.4:p.Phe405Val
ENST00000302068.8:c.1213T>G	ENSP00000306099.4:p.Phe405Val
ENST00000502545.5:n.939+461T>G
ENST00000509493.1:c.556T>G	ENSP00000426757.1:p.Phe186Val
NM_001184741.1:c.1036T>G	NP_001171670.1:p.Phe346Val
NM_005141.4:c.1213T>G , LRG_558t1:c.1213T>G	NP_005132.2:p.Phe405Val
NM_001382759.1:c.1081T>G	NP_001369688.1:p.Phe361Val
NM_001382760.1:c.1213T>G	NP_001369689.1:p.Phe405Val
NM_001382761.1:c.1213T>G	NP_001369690.1:p.Phe405Val
NM_001382762.1:c.913T>G	NP_001369691.1:p.Phe305Val
NM_001382763.1:c.1204T>G	NP_001369692.1:p.Phe402Val
NM_001382764.1:c.1081-5T>G	NP_001369693.1:n.1081-5T>G
NM_001382765.1:c.1213T>G	NP_001369694.1:p.Phe405Val
NM_005141.5:c.1213T>G MANE Select	NP_005132.2:p.Phe405Val