Canonical Allele Identifier: CA2175526786
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48495133T= , CM000677.2:g.48495133T= GRCh38
NC_000015.9:g.48787330T= , CM000677.1:g.48787330T= GRCh37
NC_000015.8:g.46574622T= NCBI36
NG_008805.2:g.155656A= , LRG_778:g.155656A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2667A= ENSP00000453958.2:p.Leu889=
ENST00000674301.2:c.2667A= ENSP00000501333.2:p.Leu889=
ENST00000684448.1:n.1341A=
ENST00000316623.10:c.2667A= MANE Select ENSP00000325527.5:p.Leu889=
ENST00000316623.9:c.2667A= ENSP00000325527.5:p.Leu889=
ENST00000537463.6:c.637-20483A= ENSP00000440294.2:n.637-20483A=
NM_000138.4:c.2667A= , LRG_778t1:c.2667A= NP_000129.3:p.Leu889=
NM_000138.5:c.2667A= MANE Select NP_000129.3:p.Leu889=