Canonical Allele Identifier: CA2175486905
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411442A= , CM000677.2:g.48411442A= GRCh38
NC_000015.9:g.48703639A= , CM000677.1:g.48703639A= GRCh37
NC_000015.8:g.46490931A= NCBI36
NG_008805.2:g.239347T= , LRG_778:g.239347T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-63T= ENSP00000453958.2:n.*1035-63T=
ENST00000674301.2:c.*1740-63T= ENSP00000501333.2:n.*1740-63T=
ENST00000682158.1:n.1608-63T=
ENST00000682170.1:n.2408-63T=
ENST00000682767.1:n.1524-63T=
ENST00000316623.10:c.8227-63T= MANE Select ENSP00000325527.5:n.8227-63T=
ENST00000674301.1:c.3393-63T= ENSP00000501333.1:n.3393-63T=
ENST00000316623.9:c.8227-63T= ENSP00000325527.5:n.8227-63T=
ENST00000559133.5:c.3596-63T=
ENST00000561429.1:n.482-63T=
NM_000138.4:c.8227-63T= , LRG_778t1:c.8227-63T= NP_000129.3:n.8227-63T=
NM_000138.5:c.8227-63T= MANE Select NP_000129.3:n.8227-63T=