Canonical Allele Identifier: CA015037
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42361
dbSNP Id: rs397515808

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48470687C>G , CM000677.2:g.48470687C>G GRCh38
NC_000015.9:g.48762884C>G , CM000677.1:g.48762884C>G GRCh37
NC_000015.8:g.46550176C>G NCBI36
NG_008805.2:g.180102G>C , LRG_778:g.180102G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4406G>C ENSP00000453958.2:p.Arg1469Pro
ENST00000674301.2:c.4406G>C ENSP00000501333.2:p.Arg1469Pro
ENST00000683268.1:n.373G>C
ENST00000684448.1:n.3080G>C
ENST00000316623.10:c.4406G>C MANE Select ENSP00000325527.5:p.Arg1469Pro
ENST00000316623.9:c.4406G>C ENSP00000325527.5:p.Arg1469Pro
ENST00000537463.6:c.*169G>C ENSP00000440294.2:n.*169G>C
NM_000138.4:c.4406G>C , LRG_778t1:c.4406G>C NP_000129.3:p.Arg1469Pro
NM_000138.5:c.4406G>C MANE Select NP_000129.3:p.Arg1469Pro