Canonical Allele Identifier: CA490090239

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48903001C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48610804C>T , CM000677.2:g.48610804C>T	GRCh38
NC_000015.9:g.48903001C>T , CM000677.1:g.48903001C>T	GRCh37
NC_000015.8:g.46690293C>T	NCBI36
NG_008805.2:g.39985G>A , LRG_778:g.39985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.270G>A	ENSP00000453958.2:p.Gly90=
ENST00000674301.2:c.270G>A	ENSP00000501333.2:p.Gly90=
ENST00000316623.10:c.270G>A MANE Select	ENSP00000325527.5:p.Gly90=
ENST00000316623.9:c.270G>A	ENSP00000325527.5:p.Gly90=
ENST00000537463.6:c.270G>A	ENSP00000440294.2:p.Gly90=
NM_000138.4:c.270G>A , LRG_778t1:c.270G>A	NP_000129.3:p.Gly90=
NM_000138.5:c.270G>A MANE Select	NP_000129.3:p.Gly90=