Canonical Allele Identifier: CA16606970
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 392364
dbSNP Id: rs1057524458

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48489988C>G , CM000677.2:g.48489988C>G GRCh38
NC_000015.9:g.48782185C>G , CM000677.1:g.48782185C>G GRCh37
NC_000015.8:g.46569477C>G NCBI36
NG_008805.2:g.160801G>C , LRG_778:g.160801G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2945G>C ENSP00000453958.2:p.Cys982Ser
ENST00000674301.2:c.2945G>C ENSP00000501333.2:p.Cys982Ser
ENST00000684448.1:n.1619G>C
ENST00000316623.10:c.2945G>C MANE Select ENSP00000325527.5:p.Cys982Ser
ENST00000316623.9:c.2945G>C ENSP00000325527.5:p.Cys982Ser
ENST00000537463.6:c.637-15338G>C ENSP00000440294.2:n.637-15338G>C
NM_000138.4:c.2945G>C , LRG_778t1:c.2945G>C NP_000129.3:p.Cys982Ser
NM_000138.5:c.2945G>C MANE Select NP_000129.3:p.Cys982Ser