Canonical Allele Identifier: CA2175510068
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48484209T= , CM000677.2:g.48484209T= GRCh38
NC_000015.9:g.48776406T= , CM000677.1:g.48776406T= GRCh37
NC_000015.8:g.46563698T= NCBI36
NG_008805.2:g.166580A= , LRG_778:g.166580A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3713-266A= ENSP00000453958.2:n.3713-266A=
ENST00000674301.2:c.3713-266A= ENSP00000501333.2:n.3713-266A=
ENST00000684448.1:n.2387-266A=
ENST00000316623.10:c.3713-266A= MANE Select ENSP00000325527.5:n.3713-266A=
ENST00000316623.9:c.3713-266A= ENSP00000325527.5:n.3713-266A=
ENST00000537463.6:c.637-9559A= ENSP00000440294.2:n.637-9559A=
NM_000138.4:c.3713-266A= , LRG_778t1:c.3713-266A= NP_000129.3:n.3713-266A=
NM_000138.5:c.3713-266A= MANE Select NP_000129.3:n.3713-266A=
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