Canonical Allele Identifier: CA2175526389
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48494397A= , CM000677.2:g.48494397A= GRCh38
NC_000015.9:g.48786594A= , CM000677.1:g.48786594A= GRCh37
NC_000015.8:g.46573886A= NCBI36
NG_008805.2:g.156392T= , LRG_778:g.156392T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.2678-143T= ENSP00000453958.2:n.2678-143T=
ENST00000674301.2:c.2678-143T= ENSP00000501333.2:n.2678-143T=
ENST00000684448.1:n.1352-143T=
ENST00000316623.10:c.2678-143T= MANE Select ENSP00000325527.5:n.2678-143T=
ENST00000316623.9:c.2678-143T= ENSP00000325527.5:n.2678-143T=
ENST00000537463.6:c.637-19747T= ENSP00000440294.2:n.637-19747T=
NM_000138.4:c.2678-143T= , LRG_778t1:c.2678-143T= NP_000129.3:n.2678-143T=
NM_000138.5:c.2678-143T= MANE Select NP_000129.3:n.2678-143T=
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