Canonical Allele Identifier: CA969579275

Gene: FBN1

Linked Data

• dbSNP Id: rs991701412
• gnomAD v3: 15-48411466-A-G
• gnomAD v4: 15-48411466-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411466A>G , CM000677.2:g.48411466A>G	GRCh38
NC_000015.9:g.48703663A>G , CM000677.1:g.48703663A>G	GRCh37
NC_000015.8:g.46490955A>G	NCBI36
NG_008805.2:g.239323T>C , LRG_778:g.239323T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1035-87T>C	ENSP00000453958.2:n.*1035-87T>C
ENST00000674301.2:c.*1740-87T>C	ENSP00000501333.2:n.*1740-87T>C
ENST00000682158.1:n.1608-87T>C
ENST00000682170.1:n.2408-87T>C
ENST00000682767.1:n.1524-87T>C
ENST00000316623.10:c.8227-87T>C MANE Select	ENSP00000325527.5:n.8227-87T>C
ENST00000674301.1:c.3393-87T>C	ENSP00000501333.1:n.3393-87T>C
ENST00000316623.9:c.8227-87T>C	ENSP00000325527.5:n.8227-87T>C
ENST00000559133.5:c.3596-87T>C
ENST00000561429.1:n.482-87T>C
NM_000138.4:c.8227-87T>C , LRG_778t1:c.8227-87T>C	NP_000129.3:n.8227-87T>C
NM_000138.5:c.8227-87T>C MANE Select	NP_000129.3:n.8227-87T>C