Canonical Allele Identifier: CA2175539220
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48537511T= , CM000677.2:g.48537511T= GRCh38
NC_000015.9:g.48829708T= , CM000677.1:g.48829708T= GRCh37
NC_000015.8:g.46617000T= NCBI36
NG_008805.2:g.113278A= , LRG_778:g.113278A=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.736+100A= ENSP00000453958.2:n.736+100A=
ENST00000674301.2:c.736+100A= ENSP00000501333.2:n.736+100A=
ENST00000316623.10:c.736+100A= MANE Select ENSP00000325527.5:n.736+100A=
ENST00000316623.9:c.736+100A= ENSP00000325527.5:n.736+100A=
ENST00000537463.6:c.636+200A= ENSP00000440294.2:n.636+200A=
NM_000138.4:c.736+100A= , LRG_778t1:c.736+100A= NP_000129.3:n.736+100A=
NM_000138.5:c.736+100A= MANE Select NP_000129.3:n.736+100A=