Canonical Allele Identifier: CA060177
Gene: FBN1 HGNC NCBI

Linked Data

dbSNP Id: rs765591910

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48411048T>G , CM000677.2:g.48411048T>G GRCh38
NC_000015.9:g.48703245T>G , CM000677.1:g.48703245T>G GRCh37
NC_000015.8:g.46490537T>G NCBI36
NG_008805.2:g.239741A>C , LRG_778:g.239741A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*1366A>C ENSP00000453958.2:n.*1366A>C
ENST00000682158.1:n.1939A>C
ENST00000682170.1:n.2739A>C
ENST00000682767.1:n.1855A>C
ENST00000316623.10:c.8558A>C MANE Select ENSP00000325527.5:p.Tyr2853Ser
ENST00000316623.9:c.8558A>C ENSP00000325527.5:p.Tyr2853Ser
ENST00000559133.5:c.3927A>C
NM_000138.4:c.8558A>C , LRG_778t1:c.8558A>C NP_000129.3:p.Tyr2853Ser
NM_000138.5:c.8558A>C MANE Select NP_000129.3:p.Tyr2853Ser