Canonical Allele Identifier: CA392320392

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48766723A>T (hg19) ; chr15:g.48474526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48474526A>T , CM000677.2:g.48474526A>T	GRCh38
NC_000015.9:g.48766723A>T , CM000677.1:g.48766723A>T	GRCh37
NC_000015.8:g.46554015A>T	NCBI36
NG_008805.2:g.176263T>A , LRG_778:g.176263T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.4087+2T>A	ENSP00000453958.2:n.4087+2T>A
ENST00000674301.2:c.4087+2T>A	ENSP00000501333.2:n.4087+2T>A
ENST00000684448.1:n.2761+2T>A
ENST00000316623.10:c.4087+2T>A MANE Select	ENSP00000325527.5:n.4087+2T>A
ENST00000316623.9:c.4087+2T>A	ENSP00000325527.5:n.4087+2T>A
ENST00000537463.6:c.759+2T>A	ENSP00000440294.2:n.759+2T>A
NM_000138.4:c.4087+2T>A , LRG_778t1:c.4087+2T>A	NP_000129.3:n.4087+2T>A
NM_000138.5:c.4087+2T>A MANE Select	NP_000129.3:n.4087+2T>A