Canonical Allele Identifier: CA2175494863
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474249A= , CM000677.2:g.48474249A= GRCh38
NC_000015.9:g.48766446A= , CM000677.1:g.48766446A= GRCh37
NC_000015.8:g.46553738A= NCBI36
NG_008805.2:g.176540T= , LRG_778:g.176540T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4210+6T= ENSP00000453958.2:n.4210+6T=
ENST00000674301.2:c.4210+6T= ENSP00000501333.2:n.4210+6T=
ENST00000684448.1:n.2884+6T=
ENST00000316623.10:c.4210+6T= MANE Select ENSP00000325527.5:n.4210+6T=
ENST00000316623.9:c.4210+6T= ENSP00000325527.5:n.4210+6T=
ENST00000537463.6:c.882+6T= ENSP00000440294.2:n.882+6T=
NM_000138.4:c.4210+6T= , LRG_778t1:c.4210+6T= NP_000129.3:n.4210+6T=
NM_000138.5:c.4210+6T= MANE Select NP_000129.3:n.4210+6T=