Canonical Allele Identifier: CA392318869

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411129-G-A
• MyVariant Identifiers: chr15:g.48703326G>A (hg19) ; chr15:g.48411129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411129G>A , CM000677.2:g.48411129G>A	GRCh38
NC_000015.9:g.48703326G>A , CM000677.1:g.48703326G>A	GRCh37
NC_000015.8:g.46490618G>A	NCBI36
NG_008805.2:g.239660C>T , LRG_778:g.239660C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1285C>T	ENSP00000453958.2:n.*1285C>T
ENST00000674301.2:c.*1990C>T	ENSP00000501333.2:n.*1990C>T
ENST00000682158.1:n.1858C>T
ENST00000682170.1:n.2658C>T
ENST00000682767.1:n.1774C>T
ENST00000316623.10:c.8477C>T MANE Select	ENSP00000325527.5:p.Thr2826Ile
ENST00000674301.1:c.3643C>T	ENSP00000501333.1:n.3643C>T
ENST00000316623.9:c.8477C>T	ENSP00000325527.5:p.Thr2826Ile
ENST00000559133.5:c.3846C>T
NM_000138.4:c.8477C>T , LRG_778t1:c.8477C>T	NP_000129.3:p.Thr2826Ile
NM_000138.5:c.8477C>T MANE Select	NP_000129.3:p.Thr2826Ile