Canonical Allele Identifier: CA392327896

Gene: FBN1

Linked Data

• ClinVar Variation Id: 449794
• ClinVar RCV Id: RCV000519976 ; RCV001219771
• dbSNP Id: rs1555394406
• MyVariant Identifiers: chr15:g.48717643C>T (hg19) ; chr15:g.48425446C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48425446C>T , CM000677.2:g.48425446C>T	GRCh38
NC_000015.9:g.48717643C>T , CM000677.1:g.48717643C>T	GRCh37
NC_000015.8:g.46504935C>T	NCBI36
NG_008805.2:g.225343G>A , LRG_778:g.225343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*184G>A	ENSP00000453958.2:n.*184G>A
ENST00000674301.2:c.*889G>A	ENSP00000501333.2:n.*889G>A
ENST00000682170.1:n.1557G>A
ENST00000682767.1:n.673G>A
ENST00000316623.10:c.7376G>A MANE Select	ENSP00000325527.5:p.Cys2459Tyr
ENST00000674301.1:c.2542G>A	ENSP00000501333.1:n.2542G>A
ENST00000316623.9:c.7376G>A	ENSP00000325527.5:p.Cys2459Tyr
ENST00000559133.5:c.2745G>A
NM_000138.4:c.7376G>A , LRG_778t1:c.7376G>A	NP_000129.3:p.Cys2459Tyr
NM_000138.5:c.7376G>A MANE Select	NP_000129.3:p.Cys2459Tyr