Canonical Allele Identifier: CA490118912

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703319T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411122T>A , CM000677.2:g.48411122T>A	GRCh38
NC_000015.9:g.48703319T>A , CM000677.1:g.48703319T>A	GRCh37
NC_000015.8:g.46490611T>A	NCBI36
NG_008805.2:g.239667A>T , LRG_778:g.239667A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1292A>T	ENSP00000453958.2:n.*1292A>T
ENST00000674301.2:c.*1997A>T	ENSP00000501333.2:n.*1997A>T
ENST00000682158.1:n.1865A>T
ENST00000682170.1:n.2665A>T
ENST00000682767.1:n.1781A>T
ENST00000316623.10:c.8484A>T MANE Select	ENSP00000325527.5:p.Ser2828=
ENST00000674301.1:c.3650A>T	ENSP00000501333.1:n.3650A>T
ENST00000316623.9:c.8484A>T	ENSP00000325527.5:p.Ser2828=
ENST00000559133.5:c.3853A>T
NM_000138.4:c.8484A>T , LRG_778t1:c.8484A>T	NP_000129.3:p.Ser2828=
NM_000138.5:c.8484A>T MANE Select	NP_000129.3:p.Ser2828=