Canonical Allele Identifier: CA442013512

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490865A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569713A>C , CM000666.2:g.154569713A>C	GRCh38
NC_000004.11:g.155490865A>C , CM000666.1:g.155490865A>C	GRCh37
NC_000004.10:g.155710315A>C	NCBI36
NG_008833.1:g.11734A>C , LRG_558:g.11734A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.1158A>C MANE Select	ENSP00000306099.4:p.Gly386=
ENST00000302068.8:c.1158A>C	ENSP00000306099.4:p.Gly386=
ENST00000502545.5:n.939+406A>C
ENST00000509493.1:c.501A>C	ENSP00000426757.1:p.Gly167=
NM_001184741.1:c.981A>C	NP_001171670.1:p.Gly327=
NM_005141.4:c.1158A>C , LRG_558t1:c.1158A>C	NP_005132.2:p.Gly386=
NM_001382759.1:c.1026A>C	NP_001369688.1:p.Gly342=
NM_001382760.1:c.1158A>C	NP_001369689.1:p.Gly386=
NM_001382761.1:c.1158A>C	NP_001369690.1:p.Gly386=
NM_001382762.1:c.858A>C	NP_001369691.1:p.Gly286=
NM_001382763.1:c.1149A>C	NP_001369692.1:p.Gly383=
NM_001382764.1:c.1081-60A>C	NP_001369693.1:n.1081-60A>C
NM_001382765.1:c.1158A>C	NP_001369694.1:p.Gly386=
NM_005141.5:c.1158A>C MANE Select	NP_005132.2:p.Gly386=