Canonical Allele Identifier: CA2175492120
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48425330C= , CM000677.2:g.48425330C= GRCh38
NC_000015.9:g.48717527C= , CM000677.1:g.48717527C= GRCh37
NC_000015.8:g.46504819C= NCBI36
NG_008805.2:g.225459G= , LRG_778:g.225459G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559133.6:c.*261+39G= ENSP00000453958.2:n.*261+39G=
ENST00000674301.2:c.*966+39G= ENSP00000501333.2:n.*966+39G=
ENST00000682170.1:n.1634+39G=
ENST00000682767.1:n.750+39G=
ENST00000316623.10:c.7453+39G= MANE Select ENSP00000325527.5:n.7453+39G=
ENST00000674301.1:c.2619+39G= ENSP00000501333.1:n.2619+39G=
ENST00000316623.9:c.7453+39G= ENSP00000325527.5:n.7453+39G=
ENST00000559133.5:c.2822+39G=
NM_000138.4:c.7453+39G= , LRG_778t1:c.7453+39G= NP_000129.3:n.7453+39G=
NM_000138.5:c.7453+39G= MANE Select NP_000129.3:n.7453+39G=