Canonical Allele Identifier: CA2175497635
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48428196T= , CM000677.2:g.48428196T= GRCh38
NC_000015.9:g.48720393T= , CM000677.1:g.48720393T= GRCh37
NC_000015.8:g.46507685T= NCBI36
NG_008805.2:g.222593A= , LRG_778:g.222593A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.6997+150A= ENSP00000453958.2:n.6997+150A=
ENST00000674301.2:c.*448+150A= ENSP00000501333.2:n.*448+150A=
ENST00000682170.1:n.756A=
ENST00000682767.1:n.232+150A=
ENST00000316623.10:c.6997+150A= MANE Select ENSP00000325527.5:n.6997+150A=
ENST00000674301.1:c.2101+150A= ENSP00000501333.1:n.2101+150A=
ENST00000316623.9:c.6997+150A= ENSP00000325527.5:n.6997+150A=
ENST00000559133.5:c.2304+150A=
ENST00000560720.1:n.434A=
NM_000138.4:c.6997+150A= , LRG_778t1:c.6997+150A= NP_000129.3:n.6997+150A=
NM_000138.5:c.6997+150A= MANE Select NP_000129.3:n.6997+150A=
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