Canonical Allele Identifier: CA2175494866
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474251A= , CM000677.2:g.48474251A= GRCh38
NC_000015.9:g.48766448A= , CM000677.1:g.48766448A= GRCh37
NC_000015.8:g.46553740A= NCBI36
NG_008805.2:g.176538T= , LRG_778:g.176538T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4210+4T= ENSP00000453958.2:n.4210+4T=
ENST00000674301.2:c.4210+4T= ENSP00000501333.2:n.4210+4T=
ENST00000684448.1:n.2884+4T=
ENST00000316623.10:c.4210+4T= MANE Select ENSP00000325527.5:n.4210+4T=
ENST00000316623.9:c.4210+4T= ENSP00000325527.5:n.4210+4T=
ENST00000537463.6:c.882+4T= ENSP00000440294.2:n.882+4T=
NM_000138.4:c.4210+4T= , LRG_778t1:c.4210+4T= NP_000129.3:n.4210+4T=
NM_000138.5:c.4210+4T= MANE Select NP_000129.3:n.4210+4T=