Canonical Allele Identifier: CA2175492811
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445483C= , CM000677.2:g.48445483C= GRCh38
NC_000015.9:g.48737680C= , CM000677.1:g.48737680C= GRCh37
NC_000015.8:g.46524972C= NCBI36
NG_008805.2:g.205306G= , LRG_778:g.205306G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.5810G= ENSP00000453958.2:p.Gly1937=
ENST00000674301.2:c.5810G= ENSP00000501333.2:p.Gly1937=
ENST00000684448.1:n.4484G=
ENST00000316623.10:c.5810G= MANE Select ENSP00000325527.5:p.Gly1937=
ENST00000674301.1:c.809G= ENSP00000501333.1:p.Gly270=
ENST00000316623.9:c.5810G= ENSP00000325527.5:p.Gly1937=
ENST00000537463.6:c.*1573G= ENSP00000440294.2:n.*1573G=
ENST00000559133.5:c.1117G=
NM_000138.4:c.5810G= , LRG_778t1:c.5810G= NP_000129.3:p.Gly1937=
NM_000138.5:c.5810G= MANE Select NP_000129.3:p.Gly1937=