Canonical Allele Identifier: CA2175526575
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48503847A= , CM000677.2:g.48503847A= GRCh38
NC_000015.9:g.48796044A= , CM000677.1:g.48796044A= GRCh37
NC_000015.8:g.46583336A= NCBI36
NG_008805.2:g.146942T= , LRG_778:g.146942T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2053T= ENSP00000453958.2:p.Cys685=
ENST00000674301.2:c.2053T= ENSP00000501333.2:p.Cys685=
ENST00000684448.1:n.727T=
ENST00000316623.10:c.2053T= MANE Select ENSP00000325527.5:p.Cys685=
ENST00000316623.9:c.2053T= ENSP00000325527.5:p.Cys685=
ENST00000537463.6:c.637-29197T= ENSP00000440294.2:n.637-29197T=
NM_000138.4:c.2053T= , LRG_778t1:c.2053T= NP_000129.3:p.Cys685=
NM_000138.5:c.2053T= MANE Select NP_000129.3:p.Cys685=