Canonical Allele Identifier: CA358508517

Gene: FGB

Linked Data

• dbSNP Id: rs958838989
• gnomAD v2: 4-155487051-G-T
• gnomAD v3: 4-154565899-G-T
• gnomAD v4: 4-154565899-G-T
• MyVariant Identifiers: chr4:g.155487051G>T (hg19) ; chr4:g.154565899G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565899G>T , CM000666.2:g.154565899G>T	GRCh38
NC_000004.11:g.155487051G>T , CM000666.1:g.155487051G>T	GRCh37
NC_000004.10:g.155706501G>T	NCBI36
NG_008833.1:g.7920G>T , LRG_558:g.7920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.206G>T MANE Select	ENSP00000306099.4:p.Gly69Val
ENST00000302068.8:c.206G>T	ENSP00000306099.4:p.Gly69Val
ENST00000425838.5:c.*118G>T	ENSP00000398719.1:n.*118G>T
ENST00000473984.1:n.119G>T
ENST00000497097.5:n.213G>T
ENST00000498375.2:n.836G>T
ENST00000502545.5:n.187G>T
ENST00000509493.1:c.-167-1694G>T	ENSP00000426757.1:n.-167-1694G>T
NM_001184741.1:c.165+41G>T	NP_001171670.1:n.165+41G>T
NM_005141.4:c.206G>T , LRG_558t1:c.206G>T	NP_005132.2:p.Gly69Val
NM_001382759.1:c.206G>T	NP_001369688.1:p.Gly69Val
NM_001382760.1:c.206G>T	NP_001369689.1:p.Gly69Val
NM_001382761.1:c.206G>T	NP_001369690.1:p.Gly69Val
NM_001382762.1:c.206G>T	NP_001369691.1:p.Gly69Val
NM_001382763.1:c.206G>T	NP_001369692.1:p.Gly69Val
NM_001382764.1:c.206G>T	NP_001369693.1:p.Gly69Val
NM_001382765.1:c.206G>T	NP_001369694.1:p.Gly69Val
NM_005141.5:c.206G>T MANE Select	NP_005132.2:p.Gly69Val