Canonical Allele Identifier: CA358515323

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490864G>C (hg19) ; chr4:g.154569712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569712G>C , CM000666.2:g.154569712G>C	GRCh38
NC_000004.11:g.155490864G>C , CM000666.1:g.155490864G>C	GRCh37
NC_000004.10:g.155710314G>C	NCBI36
NG_008833.1:g.11733G>C , LRG_558:g.11733G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1157G>C MANE Select	ENSP00000306099.4:p.Gly386Ala
ENST00000302068.8:c.1157G>C	ENSP00000306099.4:p.Gly386Ala
ENST00000502545.5:n.939+405G>C
ENST00000509493.1:c.500G>C	ENSP00000426757.1:p.Gly167Ala
NM_001184741.1:c.980G>C	NP_001171670.1:p.Gly327Ala
NM_005141.4:c.1157G>C , LRG_558t1:c.1157G>C	NP_005132.2:p.Gly386Ala
NM_001382759.1:c.1025G>C	NP_001369688.1:p.Gly342Ala
NM_001382760.1:c.1157G>C	NP_001369689.1:p.Gly386Ala
NM_001382761.1:c.1157G>C	NP_001369690.1:p.Gly386Ala
NM_001382762.1:c.857G>C	NP_001369691.1:p.Gly286Ala
NM_001382763.1:c.1148G>C	NP_001369692.1:p.Gly383Ala
NM_001382764.1:c.1081-61G>C	NP_001369693.1:n.1081-61G>C
NM_001382765.1:c.1157G>C	NP_001369694.1:p.Gly386Ala
NM_005141.5:c.1157G>C MANE Select	NP_005132.2:p.Gly386Ala