Canonical Allele Identifier: CA2175495251
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48474305T= , CM000677.2:g.48474305T= GRCh38
NC_000015.9:g.48766502T= , CM000677.1:g.48766502T= GRCh37
NC_000015.8:g.46553794T= NCBI36
NG_008805.2:g.176484A= , LRG_778:g.176484A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.4160A= ENSP00000453958.2:p.Tyr1387=
ENST00000674301.2:c.4160A= ENSP00000501333.2:p.Tyr1387=
ENST00000684448.1:n.2834A=
ENST00000316623.10:c.4160A= MANE Select ENSP00000325527.5:p.Tyr1387=
ENST00000316623.9:c.4160A= ENSP00000325527.5:p.Tyr1387=
ENST00000537463.6:c.832A= ENSP00000440294.2:p.Thr278=
NM_000138.4:c.4160A= , LRG_778t1:c.4160A= NP_000129.3:p.Tyr1387=
NM_000138.5:c.4160A= MANE Select NP_000129.3:p.Tyr1387=