Canonical Allele Identifier: CA2175484887
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48409522C= , CM000677.2:g.48409522C= GRCh38
NC_000015.9:g.48701719C= , CM000677.1:g.48701719C= GRCh37
NC_000015.8:g.46489011C= NCBI36
NG_008805.2:g.241267G= , LRG_778:g.241267G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682170.1:n.4265G=
ENST00000682767.1:n.3381G=
ENST00000316623.10:c.*1468G= MANE Select ENSP00000325527.5:n.*1468G=
ENST00000316623.9:c.*1468G= ENSP00000325527.5:n.*1468G=
NM_000138.4:c.*1468G= , LRG_778t1:c.*1468G= NP_000129.3:n.*1468G=
NM_000138.5:c.*1468G= MANE Select NP_000129.3:n.*1468G=