Canonical Allele Identifier: CA392323555
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735367

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48483823C>G , CM000677.2:g.48483823C>G GRCh38
NC_000015.9:g.48776020C>G , CM000677.1:g.48776020C>G GRCh37
NC_000015.8:g.46563312C>G NCBI36
NG_008805.2:g.166966G>C , LRG_778:g.166966G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3833G>C ENSP00000453958.2:p.Cys1278Ser
ENST00000674301.2:c.3833G>C ENSP00000501333.2:p.Cys1278Ser
ENST00000684448.1:n.2507G>C
ENST00000316623.10:c.3833G>C MANE Select ENSP00000325527.5:p.Cys1278Ser
ENST00000316623.9:c.3833G>C ENSP00000325527.5:p.Cys1278Ser
ENST00000537463.6:c.637-9173G>C ENSP00000440294.2:n.637-9173G>C
NM_000138.4:c.3833G>C , LRG_778t1:c.3833G>C NP_000129.3:p.Cys1278Ser
NM_000138.5:c.3833G>C MANE Select NP_000129.3:p.Cys1278Ser