Canonical Allele Identifier: CA2575716542
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411458A>G , CM000677.2:g.48411458A>G GRCh38
NC_000015.9:g.48703655A>G , CM000677.1:g.48703655A>G GRCh37
NC_000015.8:g.46490947A>G NCBI36
NG_008805.2:g.239331T>C , LRG_778:g.239331T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*1035-79T>C ENSP00000453958.2:n.*1035-79T>C
ENST00000674301.2:c.*1740-79T>C ENSP00000501333.2:n.*1740-79T>C
ENST00000682158.1:n.1608-79T>C
ENST00000682170.1:n.2408-79T>C
ENST00000682767.1:n.1524-79T>C
ENST00000316623.10:c.8227-79T>C MANE Select ENSP00000325527.5:n.8227-79T>C
ENST00000674301.1:c.3393-79T>C ENSP00000501333.1:n.3393-79T>C
ENST00000316623.9:c.8227-79T>C ENSP00000325527.5:n.8227-79T>C
ENST00000559133.5:c.3596-79T>C
ENST00000561429.1:n.482-79T>C
NM_000138.4:c.8227-79T>C , LRG_778t1:c.8227-79T>C NP_000129.3:n.8227-79T>C
NM_000138.5:c.8227-79T>C MANE Select NP_000129.3:n.8227-79T>C