Canonical Allele Identifier: CA2175518478
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468556T= , CM000677.2:g.48468556T= GRCh38
NC_000015.9:g.48760753T= , CM000677.1:g.48760753T= GRCh37
NC_000015.8:g.46548045T= NCBI36
NG_008805.2:g.182233A= , LRG_778:g.182233A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-22A= ENSP00000453958.2:n.4460-22A=
ENST00000674301.2:c.4460-22A= ENSP00000501333.2:n.4460-22A=
ENST00000684448.1:n.3134-22A=
ENST00000316623.10:c.4460-22A= MANE Select ENSP00000325527.5:n.4460-22A=
ENST00000316623.9:c.4460-22A= ENSP00000325527.5:n.4460-22A=
ENST00000537463.6:c.*223-22A= ENSP00000440294.2:n.*223-22A=
NM_000138.4:c.4460-22A= , LRG_778t1:c.4460-22A= NP_000129.3:n.4460-22A=
NM_000138.5:c.4460-22A= MANE Select NP_000129.3:n.4460-22A=