Canonical Allele Identifier: CA392335677

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48789508A>T (hg19) ; chr15:g.48497311A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48497311A>T , CM000677.2:g.48497311A>T	GRCh38
NC_000015.9:g.48789508A>T , CM000677.1:g.48789508A>T	GRCh37
NC_000015.8:g.46576800A>T	NCBI36
NG_008805.2:g.153478T>A , LRG_778:g.153478T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.2248T>A	ENSP00000453958.2:p.Cys750Ser
ENST00000674301.2:c.2248T>A	ENSP00000501333.2:p.Cys750Ser
ENST00000684448.1:n.922T>A
ENST00000316623.10:c.2248T>A MANE Select	ENSP00000325527.5:p.Cys750Ser
ENST00000316623.9:c.2248T>A	ENSP00000325527.5:p.Cys750Ser
ENST00000537463.6:c.637-22661T>A	ENSP00000440294.2:n.637-22661T>A
NM_000138.4:c.2248T>A , LRG_778t1:c.2248T>A	NP_000129.3:p.Cys750Ser
NM_000138.5:c.2248T>A MANE Select	NP_000129.3:p.Cys750Ser