Canonical Allele Identifier: CA441809349

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155486962T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565810T>C , CM000666.2:g.154565810T>C	GRCh38
NC_000004.11:g.155486962T>C , CM000666.1:g.155486962T>C	GRCh37
NC_000004.10:g.155706412T>C	NCBI36
NG_008833.1:g.7831T>C , LRG_558:g.7831T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.117T>C MANE Select	ENSP00000306099.4:p.Gly39=
ENST00000302068.8:c.117T>C	ENSP00000306099.4:p.Gly39=
ENST00000425838.5:c.*29T>C	ENSP00000398719.1:n.*29T>C
ENST00000473984.1:n.30T>C
ENST00000497097.5:n.124T>C
ENST00000498375.2:n.747T>C
ENST00000502545.5:n.98T>C
ENST00000509493.1:c.-167-1783T>C	ENSP00000426757.1:n.-167-1783T>C
NM_001184741.1:c.117T>C	NP_001171670.1:p.Gly39=
NM_005141.4:c.117T>C , LRG_558t1:c.117T>C	NP_005132.2:p.Gly39=
NM_001382759.1:c.117T>C	NP_001369688.1:p.Gly39=
NM_001382760.1:c.117T>C	NP_001369689.1:p.Gly39=
NM_001382761.1:c.117T>C	NP_001369690.1:p.Gly39=
NM_001382762.1:c.117T>C	NP_001369691.1:p.Gly39=
NM_001382763.1:c.117T>C	NP_001369692.1:p.Gly39=
NM_001382764.1:c.117T>C	NP_001369693.1:p.Gly39=
NM_001382765.1:c.117T>C	NP_001369694.1:p.Gly39=
NM_005141.5:c.117T>C MANE Select	NP_005132.2:p.Gly39=