Canonical Allele Identifier: CA2628324974
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410856G>T , CM000677.2:g.48410856G>T GRCh38
NC_000015.9:g.48703053G>T , CM000677.1:g.48703053G>T GRCh37
NC_000015.8:g.46490345G>T NCBI36
NG_008805.2:g.239933C>A , LRG_778:g.239933C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1558C>A ENSP00000453958.2:n.*1558C>A
ENST00000682158.1:n.2131C>A
ENST00000682170.1:n.2931C>A
ENST00000682767.1:n.2047C>A
ENST00000316623.10:c.*134C>A MANE Select ENSP00000325527.5:n.*134C>A
ENST00000316623.9:c.*134C>A ENSP00000325527.5:n.*134C>A
ENST00000559133.5:c.4119C>A
NM_000138.4:c.*134C>A , LRG_778t1:c.*134C>A NP_000129.3:n.*134C>A
NM_000138.5:c.*134C>A MANE Select NP_000129.3:n.*134C>A