Canonical Allele Identifier: CA2175497997
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448684C= , CM000677.2:g.48448684C= GRCh38
NC_000015.9:g.48740881C= , CM000677.1:g.48740881C= GRCh37
NC_000015.8:g.46528173C= NCBI36
NG_008805.2:g.202105G= , LRG_778:g.202105G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5671+84G= ENSP00000453958.2:n.5671+84G=
ENST00000674301.2:c.5671+84G= ENSP00000501333.2:n.5671+84G=
ENST00000684448.1:n.4345+84G=
ENST00000316623.10:c.5671+84G= MANE Select ENSP00000325527.5:n.5671+84G=
ENST00000674301.1:c.670+84G= ENSP00000501333.1:n.670+84G=
ENST00000316623.9:c.5671+84G= ENSP00000325527.5:n.5671+84G=
ENST00000537463.6:c.*1434+84G= ENSP00000440294.2:n.*1434+84G=
ENST00000559133.5:c.978+84G=
NM_000138.4:c.5671+84G= , LRG_778t1:c.5671+84G= NP_000129.3:n.5671+84G=
NM_000138.5:c.5671+84G= MANE Select NP_000129.3:n.5671+84G=