Canonical Allele Identifier: CA2175526775
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48495131C= , CM000677.2:g.48495131C= GRCh38
NC_000015.9:g.48787328C= , CM000677.1:g.48787328C= GRCh37
NC_000015.8:g.46574620C= NCBI36
NG_008805.2:g.155658G= , LRG_778:g.155658G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2669G= ENSP00000453958.2:p.Cys890=
ENST00000674301.2:c.2669G= ENSP00000501333.2:p.Cys890=
ENST00000684448.1:n.1343G=
ENST00000316623.10:c.2669G= MANE Select ENSP00000325527.5:p.Cys890=
ENST00000316623.9:c.2669G= ENSP00000325527.5:p.Cys890=
ENST00000537463.6:c.637-20481G= ENSP00000440294.2:n.637-20481G=
NM_000138.4:c.2669G= , LRG_778t1:c.2669G= NP_000129.3:p.Cys890=
NM_000138.5:c.2669G= MANE Select NP_000129.3:p.Cys890=