Canonical Allele Identifier: CA490119009

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703499A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411302A>T , CM000677.2:g.48411302A>T	GRCh38
NC_000015.9:g.48703499A>T , CM000677.1:g.48703499A>T	GRCh37
NC_000015.8:g.46490791A>T	NCBI36
NG_008805.2:g.239487T>A , LRG_778:g.239487T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1112T>A	ENSP00000453958.2:n.*1112T>A
ENST00000674301.2:c.*1817T>A	ENSP00000501333.2:n.*1817T>A
ENST00000682158.1:n.1685T>A
ENST00000682170.1:n.2485T>A
ENST00000682767.1:n.1601T>A
ENST00000316623.10:c.8304T>A MANE Select	ENSP00000325527.5:p.Ile2768=
ENST00000674301.1:c.3470T>A	ENSP00000501333.1:n.3470T>A
ENST00000316623.9:c.8304T>A	ENSP00000325527.5:p.Ile2768=
ENST00000559133.5:c.3673T>A
ENST00000561429.1:n.559T>A
NM_000138.4:c.8304T>A , LRG_778t1:c.8304T>A	NP_000129.3:p.Ile2768=
NM_000138.5:c.8304T>A MANE Select	NP_000129.3:p.Ile2768=