Canonical Allele Identifier: CA2175508661
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48441739T= , CM000677.2:g.48441739T= GRCh38
NC_000015.9:g.48733936T= , CM000677.1:g.48733936T= GRCh37
NC_000015.8:g.46521228T= NCBI36
NG_008805.2:g.209050A= , LRG_778:g.209050A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6145A= ENSP00000453958.2:p.Ser2049=
ENST00000674301.2:c.6145A= ENSP00000501333.2:p.Ser2049=
ENST00000316623.10:c.6145A= MANE Select ENSP00000325527.5:p.Ser2049=
ENST00000674301.1:c.1144A= ENSP00000501333.1:p.Ser382=
ENST00000316623.9:c.6145A= ENSP00000325527.5:p.Ser2049=
ENST00000537463.6:c.*1908A= ENSP00000440294.2:n.*1908A=
ENST00000559133.5:c.1452A=
ENST00000560820.1:n.265A=
NM_000138.4:c.6145A= , LRG_778t1:c.6145A= NP_000129.3:p.Ser2049=
NM_000138.5:c.6145A= MANE Select NP_000129.3:p.Ser2049=