Canonical Allele Identifier: CA490015590

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48713756T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421559T>C , CM000677.2:g.48421559T>C	GRCh38
NC_000015.9:g.48713756T>C , CM000677.1:g.48713756T>C	GRCh37
NC_000015.8:g.46501048T>C	NCBI36
NG_008805.2:g.229230A>G , LRG_778:g.229230A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*506A>G	ENSP00000453958.2:n.*506A>G
ENST00000674301.2:c.*1211A>G	ENSP00000501333.2:n.*1211A>G
ENST00000682170.1:n.1879A>G
ENST00000682767.1:n.995A>G
ENST00000316623.10:c.7698A>G MANE Select	ENSP00000325527.5:p.Glu2566=
ENST00000674301.1:c.2864A>G	ENSP00000501333.1:n.2864A>G
ENST00000316623.9:c.7698A>G	ENSP00000325527.5:p.Glu2566=
ENST00000559133.5:c.3067A>G
NM_000138.4:c.7698A>G , LRG_778t1:c.7698A>G	NP_000129.3:p.Glu2566=
NM_000138.5:c.7698A>G MANE Select	NP_000129.3:p.Glu2566=