Canonical Allele Identifier: CA2628325689
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48415533T>C , CM000677.2:g.48415533T>C GRCh38
NC_000015.9:g.48707730T>C , CM000677.1:g.48707730T>C GRCh37
NC_000015.8:g.46495022T>C NCBI36
NG_008805.2:g.235256A>G , LRG_778:g.235256A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.*859+3A>G ENSP00000453958.2:n.*859+3A>G
ENST00000674301.2:c.*1564+3A>G ENSP00000501333.2:n.*1564+3A>G
ENST00000682158.1:n.1432+3A>G
ENST00000682170.1:n.2232+3A>G
ENST00000682767.1:n.1348+3A>G
ENST00000316623.10:c.8051+3A>G MANE Select ENSP00000325527.5:n.8051+3A>G
ENST00000674301.1:c.3217+3A>G ENSP00000501333.1:n.3217+3A>G
ENST00000316623.9:c.8051+3A>G ENSP00000325527.5:n.8051+3A>G
ENST00000559133.5:c.3420+3A>G
ENST00000561429.1:n.306+3A>G
NM_000138.4:c.8051+3A>G , LRG_778t1:c.8051+3A>G NP_000129.3:n.8051+3A>G
NM_000138.5:c.8051+3A>G MANE Select NP_000129.3:n.8051+3A>G