Canonical Allele Identifier: CA2175492830
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445487T= , CM000677.2:g.48445487T= GRCh38
NC_000015.9:g.48737684T= , CM000677.1:g.48737684T= GRCh37
NC_000015.8:g.46524976T= NCBI36
NG_008805.2:g.205302A= , LRG_778:g.205302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5806A= ENSP00000453958.2:p.Ser1936=
ENST00000674301.2:c.5806A= ENSP00000501333.2:p.Ser1936=
ENST00000684448.1:n.4480A=
ENST00000316623.10:c.5806A= MANE Select ENSP00000325527.5:p.Ser1936=
ENST00000674301.1:c.805A= ENSP00000501333.1:p.Ser269=
ENST00000316623.9:c.5806A= ENSP00000325527.5:p.Ser1936=
ENST00000537463.6:c.*1569A= ENSP00000440294.2:n.*1569A=
ENST00000559133.5:c.1113A=
NM_000138.4:c.5806A= , LRG_778t1:c.5806A= NP_000129.3:p.Ser1936=
NM_000138.5:c.5806A= MANE Select NP_000129.3:p.Ser1936=