Canonical Allele Identifier: CA2175511662
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485375G= , CM000677.2:g.48485375G= GRCh38
NC_000015.9:g.48777572G= , CM000677.1:g.48777572G= GRCh37
NC_000015.8:g.46564864G= NCBI36
NG_008805.2:g.165414C= , LRG_778:g.165414C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3711C= ENSP00000453958.2:p.Thr1237=
ENST00000674301.2:c.3711C= ENSP00000501333.2:p.Thr1237=
ENST00000684448.1:n.2385C=
ENST00000316623.10:c.3711C= MANE Select ENSP00000325527.5:p.Thr1237=
ENST00000316623.9:c.3711C= ENSP00000325527.5:p.Thr1237=
ENST00000537463.6:c.637-10725C= ENSP00000440294.2:n.637-10725C=
NM_000138.4:c.3711C= , LRG_778t1:c.3711C= NP_000129.3:p.Thr1237=
NM_000138.5:c.3711C= MANE Select NP_000129.3:p.Thr1237=