Canonical Allele Identifier: CA108749998

Gene: FGB

Linked Data

• ClinVar Variation Id: 901360
• ClinVar RCV Id: RCV001147197
• dbSNP Id: rs933834957
• gnomAD v4: 4-154565903-C-T
• MyVariant Identifiers: chr4:g.155487055C>T (hg19) ; chr4:g.154565903C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565903C>T , CM000666.2:g.154565903C>T	GRCh38
NC_000004.11:g.155487055C>T , CM000666.1:g.155487055C>T	GRCh37
NC_000004.10:g.155706505C>T	NCBI36
NG_008833.1:g.7924C>T , LRG_558:g.7924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.210C>T MANE Select	ENSP00000306099.4:p.Gly70=
ENST00000302068.8:c.210C>T	ENSP00000306099.4:p.Gly70=
ENST00000425838.5:c.*122C>T	ENSP00000398719.1:n.*122C>T
ENST00000473984.1:n.123C>T
ENST00000497097.5:n.217C>T
ENST00000498375.2:n.840C>T
ENST00000502545.5:n.191C>T
ENST00000509493.1:c.-167-1690C>T	ENSP00000426757.1:n.-167-1690C>T
NM_001184741.1:c.165+45C>T	NP_001171670.1:n.165+45C>T
NM_005141.4:c.210C>T , LRG_558t1:c.210C>T	NP_005132.2:p.Gly70=
NM_001382759.1:c.210C>T	NP_001369688.1:p.Gly70=
NM_001382760.1:c.210C>T	NP_001369689.1:p.Gly70=
NM_001382761.1:c.210C>T	NP_001369690.1:p.Gly70=
NM_001382762.1:c.210C>T	NP_001369691.1:p.Gly70=
NM_001382763.1:c.210C>T	NP_001369692.1:p.Gly70=
NM_001382764.1:c.210C>T	NP_001369693.1:p.Gly70=
NM_001382765.1:c.210C>T	NP_001369694.1:p.Gly70=
NM_005141.5:c.210C>T MANE Select	NP_005132.2:p.Gly70=