Canonical Allele Identifier: CA392353718
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332760
ClinVar RCV Id: RCV001806334
dbSNP Id: rs2043341481

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468503G>C , CM000677.2:g.48468503G>C GRCh38
NC_000015.9:g.48760700G>C , CM000677.1:g.48760700G>C GRCh37
NC_000015.8:g.46547992G>C NCBI36
NG_008805.2:g.182286C>G , LRG_778:g.182286C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4491C>G ENSP00000453958.2:p.Cys1497Trp
ENST00000674301.2:c.4491C>G ENSP00000501333.2:p.Cys1497Trp
ENST00000684448.1:n.3165C>G
ENST00000316623.10:c.4491C>G MANE Select ENSP00000325527.5:p.Cys1497Trp
ENST00000316623.9:c.4491C>G ENSP00000325527.5:p.Cys1497Trp
ENST00000537463.6:c.*254C>G ENSP00000440294.2:n.*254C>G
NM_000138.4:c.4491C>G , LRG_778t1:c.4491C>G NP_000129.3:p.Cys1497Trp
NM_000138.5:c.4491C>G MANE Select NP_000129.3:p.Cys1497Trp