Canonical Allele Identifier: CA358515383

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490881G>C (hg19) ; chr4:g.154569729G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569729G>C , CM000666.2:g.154569729G>C	GRCh38
NC_000004.11:g.155490881G>C , CM000666.1:g.155490881G>C	GRCh37
NC_000004.10:g.155710331G>C	NCBI36
NG_008833.1:g.11750G>C , LRG_558:g.11750G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1174G>C MANE Select	ENSP00000306099.4:p.Gly392Arg
ENST00000302068.8:c.1174G>C	ENSP00000306099.4:p.Gly392Arg
ENST00000502545.5:n.939+422G>C
ENST00000509493.1:c.517G>C	ENSP00000426757.1:p.Gly173Arg
NM_001184741.1:c.997G>C	NP_001171670.1:p.Gly333Arg
NM_005141.4:c.1174G>C , LRG_558t1:c.1174G>C	NP_005132.2:p.Gly392Arg
NM_001382759.1:c.1042G>C	NP_001369688.1:p.Gly348Arg
NM_001382760.1:c.1174G>C	NP_001369689.1:p.Gly392Arg
NM_001382761.1:c.1174G>C	NP_001369690.1:p.Gly392Arg
NM_001382762.1:c.874G>C	NP_001369691.1:p.Gly292Arg
NM_001382763.1:c.1165G>C	NP_001369692.1:p.Gly389Arg
NM_001382764.1:c.1081-44G>C	NP_001369693.1:n.1081-44G>C
NM_001382765.1:c.1174G>C	NP_001369694.1:p.Gly392Arg
NM_005141.5:c.1174G>C MANE Select	NP_005132.2:p.Gly392Arg