Canonical Allele Identifier: CA2175492981
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48445557C= , CM000677.2:g.48445557C= GRCh38
NC_000015.9:g.48737754C= , CM000677.1:g.48737754C= GRCh37
NC_000015.8:g.46525046C= NCBI36
NG_008805.2:g.205232G= , LRG_778:g.205232G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.5789-53G= ENSP00000453958.2:n.5789-53G=
ENST00000674301.2:c.5789-53G= ENSP00000501333.2:n.5789-53G=
ENST00000684448.1:n.4463-53G=
ENST00000316623.10:c.5789-53G= MANE Select ENSP00000325527.5:n.5789-53G=
ENST00000674301.1:c.788-53G= ENSP00000501333.1:n.788-53G=
ENST00000316623.9:c.5789-53G= ENSP00000325527.5:n.5789-53G=
ENST00000537463.6:c.*1552-53G= ENSP00000440294.2:n.*1552-53G=
ENST00000559133.5:c.1096-53G=
NM_000138.4:c.5789-53G= , LRG_778t1:c.5789-53G= NP_000129.3:n.5789-53G=
NM_000138.5:c.5789-53G= MANE Select NP_000129.3:n.5789-53G=