Canonical Allele Identifier: CA490118922

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703325G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411128G>T , CM000677.2:g.48411128G>T	GRCh38
NC_000015.9:g.48703325G>T , CM000677.1:g.48703325G>T	GRCh37
NC_000015.8:g.46490617G>T	NCBI36
NG_008805.2:g.239661C>A , LRG_778:g.239661C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1286C>A	ENSP00000453958.2:n.*1286C>A
ENST00000674301.2:c.*1991C>A	ENSP00000501333.2:n.*1991C>A
ENST00000682158.1:n.1859C>A
ENST00000682170.1:n.2659C>A
ENST00000682767.1:n.1775C>A
ENST00000316623.10:c.8478C>A MANE Select	ENSP00000325527.5:p.Thr2826=
ENST00000674301.1:c.3644C>A	ENSP00000501333.1:n.3644C>A
ENST00000316623.9:c.8478C>A	ENSP00000325527.5:p.Thr2826=
ENST00000559133.5:c.3847C>A
NM_000138.4:c.8478C>A , LRG_778t1:c.8478C>A	NP_000129.3:p.Thr2826=
NM_000138.5:c.8478C>A MANE Select	NP_000129.3:p.Thr2826=