Canonical Allele Identifier: CA2175498186
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448779G= , CM000677.2:g.48448779G= GRCh38
NC_000015.9:g.48740976G= , CM000677.1:g.48740976G= GRCh37
NC_000015.8:g.46528268G= NCBI36
NG_008805.2:g.202010C= , LRG_778:g.202010C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.5660C= ENSP00000453958.2:p.Thr1887=
ENST00000674301.2:c.5660C= ENSP00000501333.2:p.Thr1887=
ENST00000684448.1:n.4334C=
ENST00000316623.10:c.5660C= MANE Select ENSP00000325527.5:p.Thr1887=
ENST00000674301.1:c.659C= ENSP00000501333.1:p.Thr220=
ENST00000316623.9:c.5660C= ENSP00000325527.5:p.Thr1887=
ENST00000537463.6:c.*1423C= ENSP00000440294.2:n.*1423C=
ENST00000559133.5:c.967C=
NM_000138.4:c.5660C= , LRG_778t1:c.5660C= NP_000129.3:p.Thr1887=
NM_000138.5:c.5660C= MANE Select NP_000129.3:p.Thr1887=