Canonical Allele Identifier: CA490014750

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48704892A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412695A>T , CM000677.2:g.48412695A>T	GRCh38
NC_000015.9:g.48704892A>T , CM000677.1:g.48704892A>T	GRCh37
NC_000015.8:g.46492184A>T	NCBI36
NG_008805.2:g.238094T>A , LRG_778:g.238094T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*908T>A	ENSP00000453958.2:n.*908T>A
ENST00000674301.2:c.*1613T>A	ENSP00000501333.2:n.*1613T>A
ENST00000682158.1:n.1481T>A
ENST00000682170.1:n.2281T>A
ENST00000682767.1:n.1397T>A
ENST00000316623.10:c.8100T>A MANE Select	ENSP00000325527.5:p.Pro2700=
ENST00000674301.1:c.3266T>A	ENSP00000501333.1:n.3266T>A
ENST00000316623.9:c.8100T>A	ENSP00000325527.5:p.Pro2700=
ENST00000559133.5:c.3469T>A
ENST00000561429.1:n.355T>A
NM_000138.4:c.8100T>A , LRG_778t1:c.8100T>A	NP_000129.3:p.Pro2700=
NM_000138.5:c.8100T>A MANE Select	NP_000129.3:p.Pro2700=