Canonical Allele Identifier: CA1504935521
Gene: FGB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154569703T= , CM000666.2:g.154569703T= GRCh38
NC_000004.11:g.155490855T= , CM000666.1:g.155490855T= GRCh37
NC_000004.10:g.155710305T= NCBI36
NG_008833.1:g.11724T= , LRG_558:g.11724T=

Transcript Alleles

HGVS Amino-acid change
ENST00000302068.9:c.1148T= MANE Select ENSP00000306099.4:p.Leu383=
ENST00000302068.8:c.1148T= ENSP00000306099.4:p.Leu383=
ENST00000502545.5:n.939+396T=
ENST00000509493.1:c.491T= ENSP00000426757.1:p.Leu164=
NM_001184741.1:c.971T= NP_001171670.1:p.Leu324=
NM_005141.4:c.1148T= , LRG_558t1:c.1148T= NP_005132.2:p.Leu383=
NM_001382759.1:c.1016T= NP_001369688.1:p.Leu339=
NM_001382760.1:c.1148T= NP_001369689.1:p.Leu383=
NM_001382761.1:c.1148T= NP_001369690.1:p.Leu383=
NM_001382762.1:c.848T= NP_001369691.1:p.Leu283=
NM_001382763.1:c.1139T= NP_001369692.1:p.Leu380=
NM_001382764.1:c.1080+68T= NP_001369693.1:n.1080+68T=
NM_001382765.1:c.1148T= NP_001369694.1:p.Leu383=
NM_005141.5:c.1148T= MANE Select NP_005132.2:p.Leu383=