Canonical Allele Identifier: CA392317911

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2773344
• ClinVar RCV Id: RCV003528027
• dbSNP Id: rs2043386208
• MyVariant Identifiers: chr15:g.48764827C>A (hg19) ; chr15:g.48472630C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48472630C>A , CM000677.2:g.48472630C>A	GRCh38
NC_000015.9:g.48764827C>A , CM000677.1:g.48764827C>A	GRCh37
NC_000015.8:g.46552119C>A	NCBI36
NG_008805.2:g.178159G>T , LRG_778:g.178159G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.4257G>T	ENSP00000453958.2:p.Gln1419His
ENST00000674301.2:c.4257G>T	ENSP00000501333.2:p.Gln1419His
ENST00000683268.1:n.224G>T
ENST00000684448.1:n.2931G>T
ENST00000316623.10:c.4257G>T MANE Select	ENSP00000325527.5:p.Gln1419His
ENST00000316623.9:c.4257G>T	ENSP00000325527.5:p.Gln1419His
ENST00000537463.6:c.*20G>T	ENSP00000440294.2:n.*20G>T
NM_000138.4:c.4257G>T , LRG_778t1:c.4257G>T	NP_000129.3:p.Gln1419His
NM_000138.5:c.4257G>T MANE Select	NP_000129.3:p.Gln1419His