Canonical Allele Identifier: CA392342224
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48448857C>G , CM000677.2:g.48448857C>G GRCh38
NC_000015.9:g.48741054C>G , CM000677.1:g.48741054C>G GRCh37
NC_000015.8:g.46528346C>G NCBI36
NG_008805.2:g.201932G>C , LRG_778:g.201932G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5582G>C ENSP00000453958.2:p.Ser1861Thr
ENST00000674301.2:c.5582G>C ENSP00000501333.2:p.Ser1861Thr
ENST00000684448.1:n.4256G>C
ENST00000316623.10:c.5582G>C MANE Select ENSP00000325527.5:p.Ser1861Thr
ENST00000674301.1:c.581G>C ENSP00000501333.1:p.Ser194Thr
ENST00000316623.9:c.5582G>C ENSP00000325527.5:p.Ser1861Thr
ENST00000537463.6:c.*1345G>C ENSP00000440294.2:n.*1345G>C
ENST00000559133.5:c.889G>C
NM_000138.4:c.5582G>C , LRG_778t1:c.5582G>C NP_000129.3:p.Ser1861Thr
NM_000138.5:c.5582G>C MANE Select NP_000129.3:p.Ser1861Thr