Canonical Allele Identifier: CA442013306

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490769T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569617T>G , CM000666.2:g.154569617T>G	GRCh38
NC_000004.11:g.155490769T>G , CM000666.1:g.155490769T>G	GRCh37
NC_000004.10:g.155710219T>G	NCBI36
NG_008833.1:g.11638T>G , LRG_558:g.11638T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1062T>G MANE Select	ENSP00000306099.4:p.Ala354=
ENST00000302068.8:c.1062T>G	ENSP00000306099.4:p.Ala354=
ENST00000502545.5:n.939+310T>G
ENST00000509493.1:c.405T>G	ENSP00000426757.1:p.Ala135=
NM_001184741.1:c.885T>G	NP_001171670.1:p.Ala295=
NM_005141.4:c.1062T>G , LRG_558t1:c.1062T>G	NP_005132.2:p.Ala354=
NM_001382759.1:c.930T>G	NP_001369688.1:p.Ala310=
NM_001382760.1:c.1062T>G	NP_001369689.1:p.Ala354=
NM_001382761.1:c.1062T>G	NP_001369690.1:p.Ala354=
NM_001382762.1:c.762T>G	NP_001369691.1:p.Ala254=
NM_001382763.1:c.1053T>G	NP_001369692.1:p.Ala351=
NM_001382764.1:c.1062T>G	NP_001369693.1:p.Ala354=
NM_001382765.1:c.1062T>G	NP_001369694.1:p.Ala354=
NM_005141.5:c.1062T>G MANE Select	NP_005132.2:p.Ala354=