Canonical Allele Identifier: CA017076
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs794728268

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48427572C>T , CM000677.2:g.48427572C>T GRCh38
NC_000015.9:g.48719769C>T , CM000677.1:g.48719769C>T GRCh37
NC_000015.8:g.46507061C>T NCBI36
NG_008805.2:g.223217G>A , LRG_778:g.223217G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*7G>A ENSP00000453958.2:n.*7G>A
ENST00000674301.2:c.*712G>A ENSP00000501333.2:n.*712G>A
ENST00000682170.1:n.1380G>A
ENST00000682767.1:n.496G>A
ENST00000316623.10:c.7199G>A MANE Select ENSP00000325527.5:p.Gly2400Glu
ENST00000674301.1:c.2365G>A ENSP00000501333.1:n.2365G>A
ENST00000316623.9:c.7199G>A ENSP00000325527.5:p.Gly2400Glu
ENST00000559133.5:c.2568G>A
NM_000138.4:c.7199G>A , LRG_778t1:c.7199G>A NP_000129.3:p.Gly2400Glu
NM_000138.5:c.7199G>A MANE Select NP_000129.3:p.Gly2400Glu