Canonical Allele Identifier: CA2175484487
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48408993G= , CM000677.2:g.48408993G= GRCh38
NC_000015.9:g.48701190G= , CM000677.1:g.48701190G= GRCh37
NC_000015.8:g.46488482G= NCBI36
NG_008805.2:g.241796C= , LRG_778:g.241796C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682170.1:n.4794C=
ENST00000682767.1:n.3910C=
ENST00000316623.10:c.*1997C= MANE Select ENSP00000325527.5:n.*1997C=
ENST00000316623.9:c.*1997C= ENSP00000325527.5:n.*1997C=
NM_000138.4:c.*1997C= , LRG_778t1:c.*1997C= NP_000129.3:n.*1997C=
NM_000138.5:c.*1997C= MANE Select NP_000129.3:n.*1997C=