Canonical Allele Identifier: CA358515558

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490926A>C (hg19) ; chr4:g.154569774A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569774A>C , CM000666.2:g.154569774A>C	GRCh38
NC_000004.11:g.155490926A>C , CM000666.1:g.155490926A>C	GRCh37
NC_000004.10:g.155710376A>C	NCBI36
NG_008833.1:g.11795A>C , LRG_558:g.11795A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1219A>C MANE Select	ENSP00000306099.4:p.Thr407Pro
ENST00000302068.8:c.1219A>C	ENSP00000306099.4:p.Thr407Pro
ENST00000502545.5:n.939+467A>C
ENST00000509493.1:c.562A>C	ENSP00000426757.1:p.Thr188Pro
NM_001184741.1:c.1042A>C	NP_001171670.1:p.Thr348Pro
NM_005141.4:c.1219A>C , LRG_558t1:c.1219A>C	NP_005132.2:p.Thr407Pro
NM_001382759.1:c.1087A>C	NP_001369688.1:p.Thr363Pro
NM_001382760.1:c.1219A>C	NP_001369689.1:p.Thr407Pro
NM_001382761.1:c.1219A>C	NP_001369690.1:p.Thr407Pro
NM_001382762.1:c.919A>C	NP_001369691.1:p.Thr307Pro
NM_001382763.1:c.1210A>C	NP_001369692.1:p.Thr404Pro
NM_001382764.1:c.1082A>C	NP_001369693.1:p.His361Pro
NM_001382765.1:c.1219A>C	NP_001369694.1:p.Thr407Pro
NM_005141.5:c.1219A>C MANE Select	NP_005132.2:p.Thr407Pro