Canonical Allele Identifier: CA490118967

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703448T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411251T>C , CM000677.2:g.48411251T>C	GRCh38
NC_000015.9:g.48703448T>C , CM000677.1:g.48703448T>C	GRCh37
NC_000015.8:g.46490740T>C	NCBI36
NG_008805.2:g.239538A>G , LRG_778:g.239538A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*1163A>G	ENSP00000453958.2:n.*1163A>G
ENST00000674301.2:c.*1868A>G	ENSP00000501333.2:n.*1868A>G
ENST00000682158.1:n.1736A>G
ENST00000682170.1:n.2536A>G
ENST00000682767.1:n.1652A>G
ENST00000316623.10:c.8355A>G MANE Select	ENSP00000325527.5:p.Thr2785=
ENST00000674301.1:c.3521A>G	ENSP00000501333.1:n.3521A>G
ENST00000316623.9:c.8355A>G	ENSP00000325527.5:p.Thr2785=
ENST00000559133.5:c.3724A>G
ENST00000561429.1:n.610A>G
NM_000138.4:c.8355A>G , LRG_778t1:c.8355A>G	NP_000129.3:p.Thr2785=
NM_000138.5:c.8355A>G MANE Select	NP_000129.3:p.Thr2785=