Canonical Allele Identifier: CA2175498337
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428432T= , CM000677.2:g.48428432T= GRCh38
NC_000015.9:g.48720629T= , CM000677.1:g.48720629T= GRCh37
NC_000015.8:g.46507921T= NCBI36
NG_008805.2:g.222357A= , LRG_778:g.222357A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6911A= ENSP00000453958.2:p.Asn2304=
ENST00000674301.2:c.*362A= ENSP00000501333.2:n.*362A=
ENST00000682170.1:n.520A=
ENST00000682767.1:n.146A=
ENST00000316623.10:c.6911A= MANE Select ENSP00000325527.5:p.Asn2304=
ENST00000674301.1:c.2015A= ENSP00000501333.1:n.2015A=
ENST00000316623.9:c.6911A= ENSP00000325527.5:p.Asn2304=
ENST00000559133.5:c.2218A=
ENST00000560720.1:n.198A=
NM_000138.4:c.6911A= , LRG_778t1:c.6911A= NP_000129.3:p.Asn2304=
NM_000138.5:c.6911A= MANE Select NP_000129.3:p.Asn2304=