Canonical Allele Identifier: CA016442

Gene: FBN1

Linked Data

• ClinVar Variation Id: 200192
• ClinVar RCV Id: RCV000181699 ; RCV001060030 ; RCV002362930 ; RCV000663870
• dbSNP Id: rs794728335
• MyVariant Identifiers: chr15:g.48729229C>T (hg19) ; chr15:g.48437032C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48437032C>T , CM000677.2:g.48437032C>T	GRCh38
NC_000015.9:g.48729229C>T , CM000677.1:g.48729229C>T	GRCh37
NC_000015.8:g.46516521C>T	NCBI36
NG_008805.2:g.213757G>A , LRG_778:g.213757G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6425G>A	ENSP00000453958.2:p.Cys2142Tyr
ENST00000674301.2:c.6425G>A	ENSP00000501333.2:p.Cys2142Tyr
ENST00000682170.1:n.34G>A
ENST00000316623.10:c.6425G>A MANE Select	ENSP00000325527.5:p.Cys2142Tyr
ENST00000674301.1:c.1424G>A	ENSP00000501333.1:p.Cys475Tyr
ENST00000316623.9:c.6425G>A	ENSP00000325527.5:p.Cys2142Tyr
ENST00000537463.6:c.*2188G>A	ENSP00000440294.2:n.*2188G>A
ENST00000559133.5:c.1732G>A
NM_000138.4:c.6425G>A , LRG_778t1:c.6425G>A	NP_000129.3:p.Cys2142Tyr
NM_000138.5:c.6425G>A MANE Select	NP_000129.3:p.Cys2142Tyr