Canonical Allele Identifier: CA392328881
Gene: FBN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48489858G>T , CM000677.2:g.48489858G>T GRCh38
NC_000015.9:g.48782055G>T , CM000677.1:g.48782055G>T GRCh37
NC_000015.8:g.46569347G>T NCBI36
NG_008805.2:g.160931C>A , LRG_778:g.160931C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.3075C>A ENSP00000453958.2:p.Phe1025Leu
ENST00000674301.2:c.3075C>A ENSP00000501333.2:p.Phe1025Leu
ENST00000684448.1:n.1749C>A
ENST00000316623.10:c.3075C>A MANE Select ENSP00000325527.5:p.Phe1025Leu
ENST00000316623.9:c.3075C>A ENSP00000325527.5:p.Phe1025Leu
ENST00000537463.6:c.637-15208C>A ENSP00000440294.2:n.637-15208C>A
NM_000138.4:c.3075C>A , LRG_778t1:c.3075C>A NP_000129.3:p.Phe1025Leu
NM_000138.5:c.3075C>A MANE Select NP_000129.3:p.Phe1025Leu