Canonical Allele Identifier: CA490022773

Gene: FBN1

Linked Data

• dbSNP Id: rs2043151992
• MyVariant Identifiers: chr15:g.48737691T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445494T>C , CM000677.2:g.48445494T>C	GRCh38
NC_000015.9:g.48737691T>C , CM000677.1:g.48737691T>C	GRCh37
NC_000015.8:g.46524983T>C	NCBI36
NG_008805.2:g.205295A>G , LRG_778:g.205295A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5799A>G	ENSP00000453958.2:p.Glu1933=
ENST00000674301.2:c.5799A>G	ENSP00000501333.2:p.Glu1933=
ENST00000684448.1:n.4473A>G
ENST00000316623.10:c.5799A>G MANE Select	ENSP00000325527.5:p.Glu1933=
ENST00000674301.1:c.798A>G	ENSP00000501333.1:p.Glu266=
ENST00000316623.9:c.5799A>G	ENSP00000325527.5:p.Glu1933=
ENST00000537463.6:c.*1562A>G	ENSP00000440294.2:n.*1562A>G
ENST00000559133.5:c.1106A>G
NM_000138.4:c.5799A>G , LRG_778t1:c.5799A>G	NP_000129.3:p.Glu1933=
NM_000138.5:c.5799A>G MANE Select	NP_000129.3:p.Glu1933=