Canonical Allele Identifier: CA2175513811
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48486925G= , CM000677.2:g.48486925G= GRCh38
NC_000015.9:g.48779122G= , CM000677.1:g.48779122G= GRCh37
NC_000015.8:g.46566414G= NCBI36
NG_008805.2:g.163864C= , LRG_778:g.163864C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.3589+150C= ENSP00000453958.2:n.3589+150C=
ENST00000674301.2:c.3589+150C= ENSP00000501333.2:n.3589+150C=
ENST00000684448.1:n.2263+150C=
ENST00000316623.10:c.3589+150C= MANE Select ENSP00000325527.5:n.3589+150C=
ENST00000316623.9:c.3589+150C= ENSP00000325527.5:n.3589+150C=
ENST00000537463.6:c.637-12275C= ENSP00000440294.2:n.637-12275C=
NM_000138.4:c.3589+150C= , LRG_778t1:c.3589+150C= NP_000129.3:n.3589+150C=
NM_000138.5:c.3589+150C= MANE Select NP_000129.3:n.3589+150C=
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