Canonical Allele Identifier: CA713391548

Gene: FBN1

Linked Data

• dbSNP Id: rs1460950091
• gnomAD v4: 15-48428041-C-A
• MyVariant Identifiers: chr15:g.48720238C>A (hg19) ; chr15:g.48428041C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428041C>A , CM000677.2:g.48428041C>A	GRCh38
NC_000015.9:g.48720238C>A , CM000677.1:g.48720238C>A	GRCh37
NC_000015.8:g.46507530C>A	NCBI36
NG_008805.2:g.222748G>T , LRG_778:g.222748G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6998-98G>T	ENSP00000453958.2:n.6998-98G>T
ENST00000674301.2:c.*449-98G>T	ENSP00000501333.2:n.*449-98G>T
ENST00000682170.1:n.911G>T
ENST00000682767.1:n.233-98G>T
ENST00000316623.10:c.6998-268G>T MANE Select	ENSP00000325527.5:n.6998-268G>T
ENST00000674301.1:c.2102-98G>T	ENSP00000501333.1:n.2102-98G>T
ENST00000316623.9:c.6998-268G>T	ENSP00000325527.5:n.6998-268G>T
ENST00000559133.5:c.2305-98G>T
ENST00000560720.1:n.589G>T
NM_000138.4:c.6998-268G>T , LRG_778t1:c.6998-268G>T	NP_000129.3:n.6998-268G>T
NM_000138.5:c.6998-268G>T MANE Select	NP_000129.3:n.6998-268G>T