Canonical Allele Identifier: CA490119156

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707789A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415592A>G , CM000677.2:g.48415592A>G	GRCh38
NC_000015.9:g.48707789A>G , CM000677.1:g.48707789A>G	GRCh37
NC_000015.8:g.46495081A>G	NCBI36
NG_008805.2:g.235197T>C , LRG_778:g.235197T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*803T>C	ENSP00000453958.2:n.*803T>C
ENST00000674301.2:c.*1508T>C	ENSP00000501333.2:n.*1508T>C
ENST00000682158.1:n.1376T>C
ENST00000682170.1:n.2176T>C
ENST00000682767.1:n.1292T>C
ENST00000316623.10:c.7995T>C MANE Select	ENSP00000325527.5:p.Asn2665=
ENST00000674301.1:c.3161T>C	ENSP00000501333.1:n.3161T>C
ENST00000316623.9:c.7995T>C	ENSP00000325527.5:p.Asn2665=
ENST00000559133.5:c.3364T>C
ENST00000561429.1:n.250T>C
NM_000138.4:c.7995T>C , LRG_778t1:c.7995T>C	NP_000129.3:p.Asn2665=
NM_000138.5:c.7995T>C MANE Select	NP_000129.3:p.Asn2665=