Canonical Allele Identifier: CA2175497334
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48434676A= , CM000677.2:g.48434676A= GRCh38
NC_000015.9:g.48726873A= , CM000677.1:g.48726873A= GRCh37
NC_000015.8:g.46514165A= NCBI36
NG_008805.2:g.216113T= , LRG_778:g.216113T=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6534T= ENSP00000453958.2:p.Asn2178=
ENST00000674301.2:c.6534T= ENSP00000501333.2:p.Asn2178=
ENST00000682170.1:n.143T=
ENST00000316623.10:c.6534T= MANE Select ENSP00000325527.5:p.Asn2178=
ENST00000674301.1:c.1533T= ENSP00000501333.1:p.Asn511=
ENST00000316623.9:c.6534T= ENSP00000325527.5:p.Asn2178=
ENST00000537463.6:c.*2297T= ENSP00000440294.2:n.*2297T=
ENST00000559133.5:c.1841T=
NM_000138.4:c.6534T= , LRG_778t1:c.6534T= NP_000129.3:p.Asn2178=
NM_000138.5:c.6534T= MANE Select NP_000129.3:p.Asn2178=