Canonical Allele Identifier: CA060163
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs765839151

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411063T>A , CM000677.2:g.48411063T>A GRCh38
NC_000015.9:g.48703260T>A , CM000677.1:g.48703260T>A GRCh37
NC_000015.8:g.46490552T>A NCBI36
NG_008805.2:g.239726A>T , LRG_778:g.239726A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1351A>T ENSP00000453958.2:n.*1351A>T
ENST00000682158.1:n.1924A>T
ENST00000682170.1:n.2724A>T
ENST00000682767.1:n.1840A>T
ENST00000316623.10:c.8543A>T MANE Select ENSP00000325527.5:p.Lys2848Ile
ENST00000316623.9:c.8543A>T ENSP00000325527.5:p.Lys2848Ile
ENST00000559133.5:c.3912A>T
NM_000138.4:c.8543A>T , LRG_778t1:c.8543A>T NP_000129.3:p.Lys2848Ile
NM_000138.5:c.8543A>T MANE Select NP_000129.3:p.Lys2848Ile