Canonical Allele Identifier: CA2175486874
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411406A= , CM000677.2:g.48411406A= GRCh38
NC_000015.9:g.48703603A= , CM000677.1:g.48703603A= GRCh37
NC_000015.8:g.46490895A= NCBI36
NG_008805.2:g.239383T= , LRG_778:g.239383T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-27T= ENSP00000453958.2:n.*1035-27T=
ENST00000674301.2:c.*1740-27T= ENSP00000501333.2:n.*1740-27T=
ENST00000682158.1:n.1608-27T=
ENST00000682170.1:n.2408-27T=
ENST00000682767.1:n.1524-27T=
ENST00000316623.10:c.8227-27T= MANE Select ENSP00000325527.5:n.8227-27T=
ENST00000674301.1:c.3393-27T= ENSP00000501333.1:n.3393-27T=
ENST00000316623.9:c.8227-27T= ENSP00000325527.5:n.8227-27T=
ENST00000559133.5:c.3596-27T=
ENST00000561429.1:n.482-27T=
NM_000138.4:c.8227-27T= , LRG_778t1:c.8227-27T= NP_000129.3:n.8227-27T=
NM_000138.5:c.8227-27T= MANE Select NP_000129.3:n.8227-27T=