Canonical Allele Identifier: CA392324359
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440223
ClinVar RCV Id: RCV001950351
dbSNP Id: rs2043497341

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485405A>C , CM000677.2:g.48485405A>C GRCh38
NC_000015.9:g.48777602A>C , CM000677.1:g.48777602A>C GRCh37
NC_000015.8:g.46564894A>C NCBI36
NG_008805.2:g.165384T>G , LRG_778:g.165384T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3681T>G ENSP00000453958.2:p.Phe1227Leu
ENST00000674301.2:c.3681T>G ENSP00000501333.2:p.Phe1227Leu
ENST00000684448.1:n.2355T>G
ENST00000316623.10:c.3681T>G MANE Select ENSP00000325527.5:p.Phe1227Leu
ENST00000316623.9:c.3681T>G ENSP00000325527.5:p.Phe1227Leu
ENST00000537463.6:c.637-10755T>G ENSP00000440294.2:n.637-10755T>G
NM_000138.4:c.3681T>G , LRG_778t1:c.3681T>G NP_000129.3:p.Phe1227Leu
NM_000138.5:c.3681T>G MANE Select NP_000129.3:p.Phe1227Leu