Canonical Allele Identifier: CA658824940
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 560347
ClinVar RCV Id: RCV000678446
dbSNP Id: rs1566897376

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441723_48441848del , CM000677.2:g.48441723_48441848del GRCh38
NC_000015.9:g.48733920_48734045del , CM000677.1:g.48733920_48734045del GRCh37
NC_000015.8:g.46521212_46521337del NCBI36
NG_008805.2:g.208943_209068del , LRG_778:g.208943_209068del

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6038_6163del
ENST00000674301.2:c.6038_6163del
ENST00000316623.10:c.6038_6163del
ENST00000674301.1:c.1037_1162del
ENST00000316623.9:c.6038_6163del
ENST00000537463.6:c.*1801_*1926del
ENST00000559133.5:c.1345_1470del
ENST00000560820.1:n.158_283del
NM_000138.4:c.6038_6163del , LRG_778t1:c.6038_6163del
NM_000138.5:c.6038_6163del