Canonical Allele Identifier: CA617832960

Gene: FBN1

Linked Data

• dbSNP Id: rs1255299553
• gnomAD v2: 15-48714486-A-T
• gnomAD v3: 15-48422289-A-T
• gnomAD v4: 15-48422289-A-T
• MyVariant Identifiers: chr15:g.48714486A>T (hg19) ; chr15:g.48422289A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48422289A>T , CM000677.2:g.48422289A>T	GRCh38
NC_000015.9:g.48714486A>T , CM000677.1:g.48714486A>T	GRCh37
NC_000015.8:g.46501778A>T	NCBI36
NG_008805.2:g.228500T>A , LRG_778:g.228500T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*262-221T>A	ENSP00000453958.2:n.*262-221T>A
ENST00000674301.2:c.*967-221T>A	ENSP00000501333.2:n.*967-221T>A
ENST00000682170.1:n.1635-221T>A
ENST00000682767.1:n.751-221T>A
ENST00000316623.10:c.7454-221T>A MANE Select	ENSP00000325527.5:n.7454-221T>A
ENST00000674301.1:c.2620-221T>A	ENSP00000501333.1:n.2620-221T>A
ENST00000316623.9:c.7454-221T>A	ENSP00000325527.5:n.7454-221T>A
ENST00000559133.5:c.2823-221T>A
NM_000138.4:c.7454-221T>A , LRG_778t1:c.7454-221T>A	NP_000129.3:n.7454-221T>A
NM_000138.5:c.7454-221T>A MANE Select	NP_000129.3:n.7454-221T>A