Canonical Allele Identifier: CA2175495690
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474447A= , CM000677.2:g.48474447A= GRCh38
NC_000015.9:g.48766644A= , CM000677.1:g.48766644A= GRCh37
NC_000015.8:g.46553936A= NCBI36
NG_008805.2:g.176342T= , LRG_778:g.176342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4088-70T= ENSP00000453958.2:n.4088-70T=
ENST00000674301.2:c.4088-70T= ENSP00000501333.2:n.4088-70T=
ENST00000684448.1:n.2762-70T=
ENST00000316623.10:c.4088-70T= MANE Select ENSP00000325527.5:n.4088-70T=
ENST00000316623.9:c.4088-70T= ENSP00000325527.5:n.4088-70T=
ENST00000537463.6:c.760-70T= ENSP00000440294.2:n.760-70T=
NM_000138.4:c.4088-70T= , LRG_778t1:c.4088-70T= NP_000129.3:n.4088-70T=
NM_000138.5:c.4088-70T= MANE Select NP_000129.3:n.4088-70T=