Canonical Allele Identifier: CA2804067558
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48420666G>T , CM000677.2:g.48420666G>T GRCh38
NC_000015.9:g.48712863G>T , CM000677.1:g.48712863G>T GRCh37
NC_000015.8:g.46500155G>T NCBI36
NG_008805.2:g.230123C>A , LRG_778:g.230123C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*627+21C>A ENSP00000453958.2:n.*627+21C>A
ENST00000674301.2:c.*1332+21C>A ENSP00000501333.2:n.*1332+21C>A
ENST00000682170.1:n.2000+21C>A
ENST00000682767.1:n.1116+21C>A
ENST00000316623.10:c.7819+21C>A MANE Select ENSP00000325527.5:n.7819+21C>A
ENST00000674301.1:c.2985+21C>A ENSP00000501333.1:n.2985+21C>A
ENST00000316623.9:c.7819+21C>A ENSP00000325527.5:n.7819+21C>A
ENST00000559133.5:c.3188+21C>A
NM_000138.4:c.7819+21C>A , LRG_778t1:c.7819+21C>A NP_000129.3:n.7819+21C>A
NM_000138.5:c.7819+21C>A MANE Select NP_000129.3:n.7819+21C>A