Canonical Allele Identifier: CA442013414

Gene: FGB

Linked Data

• gnomAD v4: 4-154569668-A-T
• MyVariant Identifiers: chr4:g.155490820A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569668A>T , CM000666.2:g.154569668A>T	GRCh38
NC_000004.11:g.155490820A>T , CM000666.1:g.155490820A>T	GRCh37
NC_000004.10:g.155710270A>T	NCBI36
NG_008833.1:g.11689A>T , LRG_558:g.11689A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1113A>T MANE Select	ENSP00000306099.4:p.Ser371=
ENST00000302068.8:c.1113A>T	ENSP00000306099.4:p.Ser371=
ENST00000502545.5:n.939+361A>T
ENST00000509493.1:c.456A>T	ENSP00000426757.1:p.Ser152=
NM_001184741.1:c.936A>T	NP_001171670.1:p.Ser312=
NM_005141.4:c.1113A>T , LRG_558t1:c.1113A>T	NP_005132.2:p.Ser371=
NM_001382759.1:c.981A>T	NP_001369688.1:p.Ser327=
NM_001382760.1:c.1113A>T	NP_001369689.1:p.Ser371=
NM_001382761.1:c.1113A>T	NP_001369690.1:p.Ser371=
NM_001382762.1:c.813A>T	NP_001369691.1:p.Ser271=
NM_001382763.1:c.1104A>T	NP_001369692.1:p.Ser368=
NM_001382764.1:c.1080+33A>T	NP_001369693.1:n.1080+33A>T
NM_001382765.1:c.1113A>T	NP_001369694.1:p.Ser371=
NM_005141.5:c.1113A>T MANE Select	NP_005132.2:p.Ser371=