Canonical Allele Identifier: CA2175484813
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48409428C= , CM000677.2:g.48409428C= GRCh38
NC_000015.9:g.48701625C= , CM000677.1:g.48701625C= GRCh37
NC_000015.8:g.46488917C= NCBI36
NG_008805.2:g.241361G= , LRG_778:g.241361G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.4359G=
ENST00000682767.1:n.3475G=
ENST00000316623.10:c.*1562G= MANE Select ENSP00000325527.5:n.*1562G=
ENST00000316623.9:c.*1562G= ENSP00000325527.5:n.*1562G=
NM_000138.4:c.*1562G= , LRG_778t1:c.*1562G= NP_000129.3:n.*1562G=
NM_000138.5:c.*1562G= MANE Select NP_000129.3:n.*1562G=