Canonical Allele Identifier: CA2175485397
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48410064G= , CM000677.2:g.48410064G= GRCh38
NC_000015.9:g.48702261G= , CM000677.1:g.48702261G= GRCh37
NC_000015.8:g.46489553G= NCBI36
NG_008805.2:g.240725C= , LRG_778:g.240725C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682170.1:n.3723C=
ENST00000682767.1:n.2839C=
ENST00000316623.10:c.*926C= MANE Select ENSP00000325527.5:n.*926C=
ENST00000316623.9:c.*926C= ENSP00000325527.5:n.*926C=
NM_000138.4:c.*926C= , LRG_778t1:c.*926C= NP_000129.3:n.*926C=
NM_000138.5:c.*926C= MANE Select NP_000129.3:n.*926C=