Canonical Allele Identifier: CA2175511783
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48444423T= , CM000677.2:g.48444423T= GRCh38
NC_000015.9:g.48736620T= , CM000677.1:g.48736620T= GRCh37
NC_000015.8:g.46523912T= NCBI36
NG_008805.2:g.206366A= , LRG_778:g.206366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6037+118A= ENSP00000453958.2:n.6037+118A=
ENST00000674301.2:c.6037+118A= ENSP00000501333.2:n.6037+118A=
ENST00000684448.1:n.4829A=
ENST00000316623.10:c.6037+118A= MANE Select ENSP00000325527.5:n.6037+118A=
ENST00000674301.1:c.1036+118A= ENSP00000501333.1:n.1036+118A=
ENST00000316623.9:c.6037+118A= ENSP00000325527.5:n.6037+118A=
ENST00000537463.6:c.*1800+118A= ENSP00000440294.2:n.*1800+118A=
ENST00000559133.5:c.1344+118A=
ENST00000560820.1:n.157+118A=
NM_000138.4:c.6037+118A= , LRG_778t1:c.6037+118A= NP_000129.3:n.6037+118A=
NM_000138.5:c.6037+118A= MANE Select NP_000129.3:n.6037+118A=
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