Canonical Allele Identifier: CA2175487827
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48412501G= , CM000677.2:g.48412501G= GRCh38
NC_000015.9:g.48704698G= , CM000677.1:g.48704698G= GRCh37
NC_000015.8:g.46491990G= NCBI36
NG_008805.2:g.238288C= , LRG_778:g.238288C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1034+68C= ENSP00000453958.2:n.*1034+68C=
ENST00000674301.2:c.*1739+68C= ENSP00000501333.2:n.*1739+68C=
ENST00000682158.1:n.1607+68C=
ENST00000682170.1:n.2407+68C=
ENST00000682767.1:n.1523+68C=
ENST00000316623.10:c.8226+68C= MANE Select ENSP00000325527.5:n.8226+68C=
ENST00000674301.1:c.3392+68C= ENSP00000501333.1:n.3392+68C=
ENST00000316623.9:c.8226+68C= ENSP00000325527.5:n.8226+68C=
ENST00000559133.5:c.3595+68C=
ENST00000561429.1:n.481+68C=
NM_000138.4:c.8226+68C= , LRG_778t1:c.8226+68C= NP_000129.3:n.8226+68C=
NM_000138.5:c.8226+68C= MANE Select NP_000129.3:n.8226+68C=