Canonical Allele Identifier: CA2175484484
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48408992C= , CM000677.2:g.48408992C= GRCh38
NC_000015.9:g.48701189C= , CM000677.1:g.48701189C= GRCh37
NC_000015.8:g.46488481C= NCBI36
NG_008805.2:g.241797G= , LRG_778:g.241797G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682170.1:n.4795G=
ENST00000682767.1:n.3911G=
ENST00000316623.10:c.*1998G= MANE Select ENSP00000325527.5:n.*1998G=
ENST00000316623.9:c.*1998G= ENSP00000325527.5:n.*1998G=
NM_000138.4:c.*1998G= , LRG_778t1:c.*1998G= NP_000129.3:n.*1998G=
NM_000138.5:c.*1998G= MANE Select NP_000129.3:n.*1998G=