Canonical Allele Identifier: CA2175498547
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448881C= , CM000677.2:g.48448881C= GRCh38
NC_000015.9:g.48741078C= , CM000677.1:g.48741078C= GRCh37
NC_000015.8:g.46528370C= NCBI36
NG_008805.2:g.201908G= , LRG_778:g.201908G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5558G= ENSP00000453958.2:p.Cys1853=
ENST00000674301.2:c.5558G= ENSP00000501333.2:p.Cys1853=
ENST00000684448.1:n.4232G=
ENST00000316623.10:c.5558G= MANE Select ENSP00000325527.5:p.Cys1853=
ENST00000674301.1:c.557G= ENSP00000501333.1:p.Cys186=
ENST00000316623.9:c.5558G= ENSP00000325527.5:p.Cys1853=
ENST00000537463.6:c.*1321G= ENSP00000440294.2:n.*1321G=
ENST00000559133.5:c.865G=
NM_000138.4:c.5558G= , LRG_778t1:c.5558G= NP_000129.3:p.Cys1853=
NM_000138.5:c.5558G= MANE Select NP_000129.3:p.Cys1853=