Canonical Allele Identifier: CA490118873

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703349T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411152T>G , CM000677.2:g.48411152T>G	GRCh38
NC_000015.9:g.48703349T>G , CM000677.1:g.48703349T>G	GRCh37
NC_000015.8:g.46490641T>G	NCBI36
NG_008805.2:g.239637A>C , LRG_778:g.239637A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1262A>C	ENSP00000453958.2:n.*1262A>C
ENST00000674301.2:c.*1967A>C	ENSP00000501333.2:n.*1967A>C
ENST00000682158.1:n.1835A>C
ENST00000682170.1:n.2635A>C
ENST00000682767.1:n.1751A>C
ENST00000316623.10:c.8454A>C MANE Select	ENSP00000325527.5:p.Thr2818=
ENST00000674301.1:c.3620A>C	ENSP00000501333.1:n.3620A>C
ENST00000316623.9:c.8454A>C	ENSP00000325527.5:p.Thr2818=
ENST00000559133.5:c.3823A>C
NM_000138.4:c.8454A>C , LRG_778t1:c.8454A>C	NP_000129.3:p.Thr2818=
NM_000138.5:c.8454A>C MANE Select	NP_000129.3:p.Thr2818=