Canonical Allele Identifier: CA392318755

Gene: FBN1

Linked Data

• ClinVar Variation Id: 1064552
• ClinVar RCV Id: RCV001374598
• dbSNP Id: rs2141209638
• MyVariant Identifiers: chr15:g.48703296A>T (hg19) ; chr15:g.48411099A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411099A>T , CM000677.2:g.48411099A>T	GRCh38
NC_000015.9:g.48703296A>T , CM000677.1:g.48703296A>T	GRCh37
NC_000015.8:g.46490588A>T	NCBI36
NG_008805.2:g.239690T>A , LRG_778:g.239690T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1315T>A	ENSP00000453958.2:n.*1315T>A
ENST00000674301.2:c.*2020T>A	ENSP00000501333.2:n.*2020T>A
ENST00000682158.1:n.1888T>A
ENST00000682170.1:n.2688T>A
ENST00000682767.1:n.1804T>A
ENST00000316623.10:c.8507T>A MANE Select	ENSP00000325527.5:p.Leu2836His
ENST00000674301.1:c.3673T>A	ENSP00000501333.1:n.3673T>A
ENST00000316623.9:c.8507T>A	ENSP00000325527.5:p.Leu2836His
ENST00000559133.5:c.3876T>A
NM_000138.4:c.8507T>A , LRG_778t1:c.8507T>A	NP_000129.3:p.Leu2836His
NM_000138.5:c.8507T>A MANE Select	NP_000129.3:p.Leu2836His