Canonical Allele Identifier: CA2175509779
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48483954T= , CM000677.2:g.48483954T= GRCh38
NC_000015.9:g.48776151T= , CM000677.1:g.48776151T= GRCh37
NC_000015.8:g.46563443T= NCBI36
NG_008805.2:g.166835A= , LRG_778:g.166835A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3713-11A= ENSP00000453958.2:n.3713-11A=
ENST00000674301.2:c.3713-11A= ENSP00000501333.2:n.3713-11A=
ENST00000684448.1:n.2387-11A=
ENST00000316623.10:c.3713-11A= MANE Select ENSP00000325527.5:n.3713-11A=
ENST00000316623.9:c.3713-11A= ENSP00000325527.5:n.3713-11A=
ENST00000537463.6:c.637-9304A= ENSP00000440294.2:n.637-9304A=
NM_000138.4:c.3713-11A= , LRG_778t1:c.3713-11A= NP_000129.3:n.3713-11A=
NM_000138.5:c.3713-11A= MANE Select NP_000129.3:n.3713-11A=