Canonical Allele Identifier: CA358515280

Gene: FGB

Linked Data

• COSMIC: COSM2156043
• MyVariant Identifiers: chr4:g.155490852C>T (hg19) ; chr4:g.154569700C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569700C>T , CM000666.2:g.154569700C>T	GRCh38
NC_000004.11:g.155490852C>T , CM000666.1:g.155490852C>T	GRCh37
NC_000004.10:g.155710302C>T	NCBI36
NG_008833.1:g.11721C>T , LRG_558:g.11721C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1145C>T MANE Select	ENSP00000306099.4:p.Ala382Val
ENST00000302068.8:c.1145C>T	ENSP00000306099.4:p.Ala382Val
ENST00000502545.5:n.939+393C>T
ENST00000509493.1:c.488C>T	ENSP00000426757.1:p.Ala163Val
NM_001184741.1:c.968C>T	NP_001171670.1:p.Ala323Val
NM_005141.4:c.1145C>T , LRG_558t1:c.1145C>T	NP_005132.2:p.Ala382Val
NM_001382759.1:c.1013C>T	NP_001369688.1:p.Ala338Val
NM_001382760.1:c.1145C>T	NP_001369689.1:p.Ala382Val
NM_001382761.1:c.1145C>T	NP_001369690.1:p.Ala382Val
NM_001382762.1:c.845C>T	NP_001369691.1:p.Ala282Val
NM_001382763.1:c.1136C>T	NP_001369692.1:p.Ala379Val
NM_001382764.1:c.1080+65C>T	NP_001369693.1:n.1080+65C>T
NM_001382765.1:c.1145C>T	NP_001369694.1:p.Ala382Val
NM_005141.5:c.1145C>T MANE Select	NP_005132.2:p.Ala382Val