Canonical Allele Identifier: CA392331591
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 549107
ClinVar RCV Id: RCV000663574
dbSNP Id: rs1057523406

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48494209C>A , CM000677.2:g.48494209C>A GRCh38
NC_000015.9:g.48786406C>A , CM000677.1:g.48786406C>A GRCh37
NC_000015.8:g.46573698C>A NCBI36
NG_008805.2:g.156580G>T , LRG_778:g.156580G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2723G>T ENSP00000453958.2:p.Cys908Phe
ENST00000674301.2:c.2723G>T ENSP00000501333.2:p.Cys908Phe
ENST00000684448.1:n.1397G>T
ENST00000316623.10:c.2723G>T MANE Select ENSP00000325527.5:p.Cys908Phe
ENST00000316623.9:c.2723G>T ENSP00000325527.5:p.Cys908Phe
ENST00000537463.6:c.637-19559G>T ENSP00000440294.2:n.637-19559G>T
NM_000138.4:c.2723G>T , LRG_778t1:c.2723G>T NP_000129.3:p.Cys908Phe
NM_000138.5:c.2723G>T MANE Select NP_000129.3:p.Cys908Phe