Canonical Allele Identifier: CA392337958

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2942000
• ClinVar RCV Id: RCV003803022
• MyVariant Identifiers: chr15:g.48733930T>A (hg19) ; chr15:g.48441733T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48441733T>A , CM000677.2:g.48441733T>A	GRCh38
NC_000015.9:g.48733930T>A , CM000677.1:g.48733930T>A	GRCh37
NC_000015.8:g.46521222T>A	NCBI36
NG_008805.2:g.209056A>T , LRG_778:g.209056A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6151A>T	ENSP00000453958.2:p.Arg2051Ter
ENST00000674301.2:c.6151A>T	ENSP00000501333.2:p.Arg2051Ter
ENST00000316623.10:c.6151A>T MANE Select	ENSP00000325527.5:p.Arg2051Ter
ENST00000674301.1:c.1150A>T	ENSP00000501333.1:p.Arg384Ter
ENST00000316623.9:c.6151A>T	ENSP00000325527.5:p.Arg2051Ter
ENST00000537463.6:c.*1914A>T	ENSP00000440294.2:n.*1914A>T
ENST00000559133.5:c.1458A>T
ENST00000560820.1:n.271A>T
NM_000138.4:c.6151A>T , LRG_778t1:c.6151A>T	NP_000129.3:p.Arg2051Ter
NM_000138.5:c.6151A>T MANE Select	NP_000129.3:p.Arg2051Ter