Canonical Allele Identifier: CA392339674

Gene: FBN1

Linked Data

• ClinVar Variation Id: 521729
• ClinVar RCV Id: RCV002532843 ; RCV004025276
• dbSNP Id: rs1555395645
• MyVariant Identifiers: chr15:g.48736776C>T (hg19) ; chr15:g.48444579C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48444579C>T , CM000677.2:g.48444579C>T	GRCh38
NC_000015.9:g.48736776C>T , CM000677.1:g.48736776C>T	GRCh37
NC_000015.8:g.46524068C>T	NCBI36
NG_008805.2:g.206210G>A , LRG_778:g.206210G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5999G>A	ENSP00000453958.2:p.Cys2000Tyr
ENST00000674301.2:c.5999G>A	ENSP00000501333.2:p.Cys2000Tyr
ENST00000684448.1:n.4673G>A
ENST00000316623.10:c.5999G>A MANE Select	ENSP00000325527.5:p.Cys2000Tyr
ENST00000674301.1:c.998G>A	ENSP00000501333.1:p.Cys333Tyr
ENST00000316623.9:c.5999G>A	ENSP00000325527.5:p.Cys2000Tyr
ENST00000537463.6:c.*1762G>A	ENSP00000440294.2:n.*1762G>A
ENST00000559133.5:c.1306G>A
ENST00000560820.1:n.119G>A
NM_000138.4:c.5999G>A , LRG_778t1:c.5999G>A	NP_000129.3:p.Cys2000Tyr
NM_000138.5:c.5999G>A MANE Select	NP_000129.3:p.Cys2000Tyr