Canonical Allele Identifier: CA2175485958
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410744T= , CM000677.2:g.48410744T= GRCh38
NC_000015.9:g.48702941T= , CM000677.1:g.48702941T= GRCh37
NC_000015.8:g.46490233T= NCBI36
NG_008805.2:g.240045A= , LRG_778:g.240045A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1670A= ENSP00000453958.2:n.*1670A=
ENST00000682158.1:n.2243A=
ENST00000682170.1:n.3043A=
ENST00000682767.1:n.2159A=
ENST00000316623.10:c.*246A= MANE Select ENSP00000325527.5:n.*246A=
ENST00000316623.9:c.*246A= ENSP00000325527.5:n.*246A=
ENST00000559133.5:c.4231A=
NM_000138.4:c.*246A= , LRG_778t1:c.*246A= NP_000129.3:n.*246A=
NM_000138.5:c.*246A= MANE Select NP_000129.3:n.*246A=