Canonical Allele Identifier: CA392323342

Gene: FBN1

Linked Data

• ClinVar Variation Id: 449756
• ClinVar RCV Id: RCV000522194 ; RCV002413405 ; RCV003766945
• dbSNP Id: rs1555393875
• MyVariant Identifiers: chr15:g.48707904C>T (hg19) ; chr15:g.48415707C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415707C>T , CM000677.2:g.48415707C>T	GRCh38
NC_000015.9:g.48707904C>T , CM000677.1:g.48707904C>T	GRCh37
NC_000015.8:g.46495196C>T	NCBI36
NG_008805.2:g.235082G>A , LRG_778:g.235082G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*688G>A	ENSP00000453958.2:n.*688G>A
ENST00000674301.2:c.*1393G>A	ENSP00000501333.2:n.*1393G>A
ENST00000682158.1:n.1261G>A
ENST00000682170.1:n.2061G>A
ENST00000682767.1:n.1177G>A
ENST00000316623.10:c.7880G>A MANE Select	ENSP00000325527.5:p.Gly2627Glu
ENST00000674301.1:c.3046G>A	ENSP00000501333.1:n.3046G>A
ENST00000316623.9:c.7880G>A	ENSP00000325527.5:p.Gly2627Glu
ENST00000559133.5:c.3249G>A
ENST00000561429.1:n.135G>A
NM_000138.4:c.7880G>A , LRG_778t1:c.7880G>A	NP_000129.3:p.Gly2627Glu
NM_000138.5:c.7880G>A MANE Select	NP_000129.3:p.Gly2627Glu