Canonical Allele Identifier: CA358515584

Gene: FGB

Linked Data

• MyVariant Identifiers: chr4:g.155490932G>T (hg19) ; chr4:g.154569780G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569780G>T , CM000666.2:g.154569780G>T	GRCh38
NC_000004.11:g.155490932G>T , CM000666.1:g.155490932G>T	GRCh37
NC_000004.10:g.155710382G>T	NCBI36
NG_008833.1:g.11801G>T , LRG_558:g.11801G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1225G>T MANE Select	ENSP00000306099.4:p.Asp409Tyr
ENST00000302068.8:c.1225G>T	ENSP00000306099.4:p.Asp409Tyr
ENST00000502545.5:n.939+473G>T
ENST00000509493.1:c.568G>T	ENSP00000426757.1:p.Asp190Tyr
NM_001184741.1:c.1048G>T	NP_001171670.1:p.Asp350Tyr
NM_005141.4:c.1225G>T , LRG_558t1:c.1225G>T	NP_005132.2:p.Asp409Tyr
NM_001382759.1:c.1093G>T	NP_001369688.1:p.Asp365Tyr
NM_001382760.1:c.1225G>T	NP_001369689.1:p.Asp409Tyr
NM_001382761.1:c.1225G>T	NP_001369690.1:p.Asp409Tyr
NM_001382762.1:c.925G>T	NP_001369691.1:p.Asp309Tyr
NM_001382763.1:c.1216G>T	NP_001369692.1:p.Asp406Tyr
NM_001382764.1:c.1088G>T	NP_001369693.1:p.Ter363Leu
NM_001382765.1:c.1220+5G>T	NP_001369694.1:n.1220+5G>T
NM_005141.5:c.1225G>T MANE Select	NP_005132.2:p.Asp409Tyr