Canonical Allele Identifier: CA358515610

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490938G>T (hg19) ; chr4:g.154569786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569786G>T , CM000666.2:g.154569786G>T	GRCh38
NC_000004.11:g.155490938G>T , CM000666.1:g.155490938G>T	GRCh37
NC_000004.10:g.155710388G>T	NCBI36
NG_008833.1:g.11807G>T , LRG_558:g.11807G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1231G>T MANE Select	ENSP00000306099.4:p.Asp411Tyr
ENST00000302068.8:c.1231G>T	ENSP00000306099.4:p.Asp411Tyr
ENST00000502545.5:n.939+479G>T
ENST00000509493.1:c.574G>T	ENSP00000426757.1:p.Asp192Tyr
NM_001184741.1:c.1054G>T	NP_001171670.1:p.Asp352Tyr
NM_005141.4:c.1231G>T , LRG_558t1:c.1231G>T	NP_005132.2:p.Asp411Tyr
NM_001382759.1:c.1099G>T	NP_001369688.1:p.Asp367Tyr
NM_001382760.1:c.1231G>T	NP_001369689.1:p.Asp411Tyr
NM_001382761.1:c.1231G>T	NP_001369690.1:p.Asp411Tyr
NM_001382762.1:c.931G>T	NP_001369691.1:p.Asp311Tyr
NM_001382763.1:c.1222G>T	NP_001369692.1:p.Asp408Tyr
NM_001382764.1:c.*5G>T	NP_001369693.1:n.*5G>T
NM_001382765.1:c.1220+11G>T	NP_001369694.1:n.1220+11G>T
NM_005141.5:c.1231G>T MANE Select	NP_005132.2:p.Asp411Tyr