Canonical Allele Identifier: CA2175502828
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48430770A= , CM000677.2:g.48430770A= GRCh38
NC_000015.9:g.48722967A= , CM000677.1:g.48722967A= GRCh37
NC_000015.8:g.46510259A= NCBI36
NG_008805.2:g.220019T= , LRG_778:g.220019T=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.6772T= ENSP00000453958.2:p.Cys2258=
ENST00000674301.2:c.*223T= ENSP00000501333.2:n.*223T=
ENST00000682170.1:n.381T=
ENST00000316623.10:c.6772T= MANE Select ENSP00000325527.5:p.Cys2258=
ENST00000674301.1:c.1876T= ENSP00000501333.1:n.1876T=
ENST00000316623.9:c.6772T= ENSP00000325527.5:p.Cys2258=
ENST00000537463.6:c.*2535T= ENSP00000440294.2:n.*2535T=
ENST00000559133.5:c.2079T=
ENST00000560720.1:n.59T=
NM_000138.4:c.6772T= , LRG_778t1:c.6772T= NP_000129.3:p.Cys2258=
NM_000138.5:c.6772T= MANE Select NP_000129.3:p.Cys2258=