Canonical Allele Identifier: CA490018792

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48726894A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434697A>T , CM000677.2:g.48434697A>T	GRCh38
NC_000015.9:g.48726894A>T , CM000677.1:g.48726894A>T	GRCh37
NC_000015.8:g.46514186A>T	NCBI36
NG_008805.2:g.216092T>A , LRG_778:g.216092T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6513T>A	ENSP00000453958.2:p.Ser2171=
ENST00000674301.2:c.6513T>A	ENSP00000501333.2:p.Ser2171=
ENST00000682170.1:n.122T>A
ENST00000316623.10:c.6513T>A MANE Select	ENSP00000325527.5:p.Ser2171=
ENST00000674301.1:c.1512T>A	ENSP00000501333.1:p.Ser504=
ENST00000316623.9:c.6513T>A	ENSP00000325527.5:p.Ser2171=
ENST00000537463.6:c.*2276T>A	ENSP00000440294.2:n.*2276T>A
ENST00000559133.5:c.1820T>A
NM_000138.4:c.6513T>A , LRG_778t1:c.6513T>A	NP_000129.3:p.Ser2171=
NM_000138.5:c.6513T>A MANE Select	NP_000129.3:p.Ser2171=