Canonical Allele Identifier: CA2175511549
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48485316A= , CM000677.2:g.48485316A= GRCh38
NC_000015.9:g.48777513A= , CM000677.1:g.48777513A= GRCh37
NC_000015.8:g.46564805A= NCBI36
NG_008805.2:g.165473T= , LRG_778:g.165473T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3712+58T= ENSP00000453958.2:n.3712+58T=
ENST00000674301.2:c.3712+58T= ENSP00000501333.2:n.3712+58T=
ENST00000684448.1:n.2386+58T=
ENST00000316623.10:c.3712+58T= MANE Select ENSP00000325527.5:n.3712+58T=
ENST00000316623.9:c.3712+58T= ENSP00000325527.5:n.3712+58T=
ENST00000537463.6:c.637-10666T= ENSP00000440294.2:n.637-10666T=
NM_000138.4:c.3712+58T= , LRG_778t1:c.3712+58T= NP_000129.3:n.3712+58T=
NM_000138.5:c.3712+58T= MANE Select NP_000129.3:n.3712+58T=