Canonical Allele Identifier: CA969549011
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs2043115795

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441647G>A , CM000677.2:g.48441647G>A GRCh38
NC_000015.9:g.48733844G>A , CM000677.1:g.48733844G>A GRCh37
NC_000015.8:g.46521136G>A NCBI36
NG_008805.2:g.209142C>T , LRG_778:g.209142C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6163+74C>T ENSP00000453958.2:n.6163+74C>T
ENST00000674301.2:c.6163+74C>T ENSP00000501333.2:n.6163+74C>T
ENST00000316623.10:c.6163+74C>T MANE Select ENSP00000325527.5:n.6163+74C>T
ENST00000674301.1:c.1162+74C>T ENSP00000501333.1:n.1162+74C>T
ENST00000316623.9:c.6163+74C>T ENSP00000325527.5:n.6163+74C>T
ENST00000537463.6:c.*1926+74C>T ENSP00000440294.2:n.*1926+74C>T
ENST00000559133.5:c.1470+74C>T
ENST00000560820.1:n.283+74C>T
NM_000138.4:c.6163+74C>T , LRG_778t1:c.6163+74C>T NP_000129.3:n.6163+74C>T
NM_000138.5:c.6163+74C>T MANE Select NP_000129.3:n.6163+74C>T