Canonical Allele Identifier: CA2175516156
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48488354G= , CM000677.2:g.48488354G= GRCh38
NC_000015.9:g.48780551G= , CM000677.1:g.48780551G= GRCh37
NC_000015.8:g.46567843G= NCBI36
NG_008805.2:g.162435C= , LRG_778:g.162435C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3208+14C= ENSP00000453958.2:n.3208+14C=
ENST00000674301.2:c.3208+14C= ENSP00000501333.2:n.3208+14C=
ENST00000684448.1:n.1882+14C=
ENST00000316623.10:c.3208+14C= MANE Select ENSP00000325527.5:n.3208+14C=
ENST00000316623.9:c.3208+14C= ENSP00000325527.5:n.3208+14C=
ENST00000537463.6:c.637-13704C= ENSP00000440294.2:n.637-13704C=
NM_000138.4:c.3208+14C= , LRG_778t1:c.3208+14C= NP_000129.3:n.3208+14C=
NM_000138.5:c.3208+14C= MANE Select NP_000129.3:n.3208+14C=