Canonical Allele Identifier: CA915946648
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 684602
ClinVar RCV Id: RCV000984069
dbSNP Id: rs1597525871

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48436961del , CM000677.2:g.48436961del GRCh38
NC_000015.9:g.48729158del , CM000677.1:g.48729158del GRCh37
NC_000015.8:g.46516450del NCBI36
NG_008805.2:g.213829del , LRG_778:g.213829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6496+1del
ENST00000674301.2:c.6496+1del
ENST00000682170.1:n.105+1del
ENST00000316623.10:c.6496+1del
ENST00000674301.1:c.1495+1del
ENST00000316623.9:c.6496+1del
ENST00000537463.6:c.*2259+1del
ENST00000559133.5:c.1803+1del
NM_000138.4:c.6496+1del , LRG_778t1:c.6496+1del
NM_000138.5:c.6496+1del