Canonical Allele Identifier: CA2175518519
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48468635T= , CM000677.2:g.48468635T= GRCh38
NC_000015.9:g.48760832T= , CM000677.1:g.48760832T= GRCh37
NC_000015.8:g.46548124T= NCBI36
NG_008805.2:g.182154A= , LRG_778:g.182154A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4460-101A= ENSP00000453958.2:n.4460-101A=
ENST00000674301.2:c.4460-101A= ENSP00000501333.2:n.4460-101A=
ENST00000684448.1:n.3134-101A=
ENST00000316623.10:c.4460-101A= MANE Select ENSP00000325527.5:n.4460-101A=
ENST00000316623.9:c.4460-101A= ENSP00000325527.5:n.4460-101A=
ENST00000537463.6:c.*223-101A= ENSP00000440294.2:n.*223-101A=
NM_000138.4:c.4460-101A= , LRG_778t1:c.4460-101A= NP_000129.3:n.4460-101A=
NM_000138.5:c.4460-101A= MANE Select NP_000129.3:n.4460-101A=