Canonical Allele Identifier: CA10587805

Gene: FBN1

Linked Data

• ClinVar Variation Id: 264106
• ClinVar RCV Id: RCV002310990
• dbSNP Id: rs886039047
• MyVariant Identifiers: chr15:g.48722966C>T (hg19) ; chr15:g.48430769C>T (hg38)
• PubMed: PMID:10647894

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48430769C>T , CM000677.2:g.48430769C>T	GRCh38
NC_000015.9:g.48722966C>T , CM000677.1:g.48722966C>T	GRCh37
NC_000015.8:g.46510258C>T	NCBI36
NG_008805.2:g.220020G>A , LRG_778:g.220020G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.6773G>A	ENSP00000453958.2:p.Cys2258Tyr
ENST00000674301.2:c.*224G>A	ENSP00000501333.2:n.*224G>A
ENST00000682170.1:n.382G>A
ENST00000316623.10:c.6773G>A MANE Select	ENSP00000325527.5:p.Cys2258Tyr
ENST00000674301.1:c.1877G>A	ENSP00000501333.1:n.1877G>A
ENST00000316623.9:c.6773G>A	ENSP00000325527.5:p.Cys2258Tyr
ENST00000537463.6:c.*2536G>A	ENSP00000440294.2:n.*2536G>A
ENST00000559133.5:c.2080G>A
ENST00000560720.1:n.60G>A
NM_000138.4:c.6773G>A , LRG_778t1:c.6773G>A	NP_000129.3:p.Cys2258Tyr
NM_000138.5:c.6773G>A MANE Select	NP_000129.3:p.Cys2258Tyr