Canonical Allele Identifier: CA269519899

Gene: FBN1

Linked Data

• dbSNP Id: rs557170930
• MyVariant Identifiers: chr15:g.48713998T>A (hg19) ; chr15:g.48421801T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421801T>A , CM000677.2:g.48421801T>A	GRCh38
NC_000015.9:g.48713998T>A , CM000677.1:g.48713998T>A	GRCh37
NC_000015.8:g.46501290T>A	NCBI36
NG_008805.2:g.228988A>T , LRG_778:g.228988A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*379-115A>T	ENSP00000453958.2:n.*379-115A>T
ENST00000674301.2:c.*1084-115A>T	ENSP00000501333.2:n.*1084-115A>T
ENST00000682170.1:n.1752-115A>T
ENST00000682767.1:n.868-115A>T
ENST00000316623.10:c.7571-115A>T MANE Select	ENSP00000325527.5:n.7571-115A>T
ENST00000674301.1:c.2737-115A>T	ENSP00000501333.1:n.2737-115A>T
ENST00000316623.9:c.7571-115A>T	ENSP00000325527.5:n.7571-115A>T
ENST00000559133.5:c.2940-115A>T
NM_000138.4:c.7571-115A>T , LRG_778t1:c.7571-115A>T	NP_000129.3:n.7571-115A>T
NM_000138.5:c.7571-115A>T MANE Select	NP_000129.3:n.7571-115A>T