Canonical Allele Identifier: CA392317743
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 549216
dbSNP Id: rs1555397545

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48472601C>T , CM000677.2:g.48472601C>T GRCh38
NC_000015.9:g.48764798C>T , CM000677.1:g.48764798C>T GRCh37
NC_000015.8:g.46552090C>T NCBI36
NG_008805.2:g.178188G>A , LRG_778:g.178188G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4286G>A ENSP00000453958.2:p.Cys1429Tyr
ENST00000674301.2:c.4286G>A ENSP00000501333.2:p.Cys1429Tyr
ENST00000683268.1:n.253G>A
ENST00000684448.1:n.2960G>A
ENST00000316623.10:c.4286G>A MANE Select ENSP00000325527.5:p.Cys1429Tyr
ENST00000316623.9:c.4286G>A ENSP00000325527.5:p.Cys1429Tyr
ENST00000537463.6:c.*49G>A ENSP00000440294.2:n.*49G>A
NM_000138.4:c.4286G>A , LRG_778t1:c.4286G>A NP_000129.3:p.Cys1429Tyr
NM_000138.5:c.4286G>A MANE Select NP_000129.3:p.Cys1429Tyr