Canonical Allele Identifier: CA2628331298
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428093C>A , CM000677.2:g.48428093C>A GRCh38
NC_000015.9:g.48720290C>A , CM000677.1:g.48720290C>A GRCh37
NC_000015.8:g.46507582C>A NCBI36
NG_008805.2:g.222696G>T , LRG_778:g.222696G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6998-150G>T ENSP00000453958.2:n.6998-150G>T
ENST00000674301.2:c.*449-150G>T ENSP00000501333.2:n.*449-150G>T
ENST00000682170.1:n.859G>T
ENST00000682767.1:n.233-150G>T
ENST00000316623.10:c.6997+253G>T MANE Select ENSP00000325527.5:n.6997+253G>T
ENST00000674301.1:c.2102-150G>T ENSP00000501333.1:n.2102-150G>T
ENST00000316623.9:c.6997+253G>T ENSP00000325527.5:n.6997+253G>T
ENST00000559133.5:c.2305-150G>T
ENST00000560720.1:n.537G>T
NM_000138.4:c.6997+253G>T , LRG_778t1:c.6997+253G>T NP_000129.3:n.6997+253G>T
NM_000138.5:c.6997+253G>T MANE Select NP_000129.3:n.6997+253G>T