Canonical Allele Identifier: CA618009232

Gene: FBN1

Linked Data

• ClinVar Variation Id: 922714
• ClinVar RCV Id: RCV001182903 ; RCV002559815
• dbSNP Id: rs1365010331
• gnomAD v2: 15-48714269-C-A
• gnomAD v4: 15-48422072-C-A
• MyVariant Identifiers: chr15:g.48714269C>A (hg19) ; chr15:g.48422072C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422072C>A , CM000677.2:g.48422072C>A	GRCh38
NC_000015.9:g.48714269C>A , CM000677.1:g.48714269C>A	GRCh37
NC_000015.8:g.46501561C>A	NCBI36
NG_008805.2:g.228717G>T , LRG_778:g.228717G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*262-4G>T	ENSP00000453958.2:n.*262-4G>T
ENST00000674301.2:c.*967-4G>T	ENSP00000501333.2:n.*967-4G>T
ENST00000682170.1:n.1635-4G>T
ENST00000682767.1:n.751-4G>T
ENST00000316623.10:c.7454-4G>T MANE Select	ENSP00000325527.5:n.7454-4G>T
ENST00000674301.1:c.2620-4G>T	ENSP00000501333.1:n.2620-4G>T
ENST00000316623.9:c.7454-4G>T	ENSP00000325527.5:n.7454-4G>T
ENST00000559133.5:c.2823-4G>T
NM_000138.4:c.7454-4G>T , LRG_778t1:c.7454-4G>T	NP_000129.3:n.7454-4G>T
NM_000138.5:c.7454-4G>T MANE Select	NP_000129.3:n.7454-4G>T