Canonical Allele Identifier: CA2175494971
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48446737A= , CM000677.2:g.48446737A= GRCh38
NC_000015.9:g.48738934A= , CM000677.1:g.48738934A= GRCh37
NC_000015.8:g.46526226A= NCBI36
NG_008805.2:g.204052T= , LRG_778:g.204052T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5757T= ENSP00000453958.2:p.Gly1919=
ENST00000674301.2:c.5757T= ENSP00000501333.2:p.Gly1919=
ENST00000684448.1:n.4431T=
ENST00000316623.10:c.5757T= MANE Select ENSP00000325527.5:p.Gly1919=
ENST00000674301.1:c.756T= ENSP00000501333.1:p.Gly252=
ENST00000316623.9:c.5757T= ENSP00000325527.5:p.Gly1919=
ENST00000537463.6:c.*1520T= ENSP00000440294.2:n.*1520T=
ENST00000559133.5:c.1064T=
NM_000138.4:c.5757T= , LRG_778t1:c.5757T= NP_000129.3:p.Gly1919=
NM_000138.5:c.5757T= MANE Select NP_000129.3:p.Gly1919=