Canonical Allele Identifier: CA2175526644
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48503883G= , CM000677.2:g.48503883G= GRCh38
NC_000015.9:g.48796080G= , CM000677.1:g.48796080G= GRCh37
NC_000015.8:g.46583372G= NCBI36
NG_008805.2:g.146906C= , LRG_778:g.146906C=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.2017C= ENSP00000453958.2:p.Pro673=
ENST00000674301.2:c.2017C= ENSP00000501333.2:p.Pro673=
ENST00000684448.1:n.691C=
ENST00000316623.10:c.2017C= MANE Select ENSP00000325527.5:p.Pro673=
ENST00000316623.9:c.2017C= ENSP00000325527.5:p.Pro673=
ENST00000537463.6:c.637-29233C= ENSP00000440294.2:n.637-29233C=
NM_000138.4:c.2017C= , LRG_778t1:c.2017C= NP_000129.3:p.Pro673=
NM_000138.5:c.2017C= MANE Select NP_000129.3:p.Pro673=