Canonical Allele Identifier: CA490018732

Gene: FBN1

Linked Data

• dbSNP Id: rs111844882
• MyVariant Identifiers: chr15:g.48726813G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48434616G>T , CM000677.2:g.48434616G>T	GRCh38
NC_000015.9:g.48726813G>T , CM000677.1:g.48726813G>T	GRCh37
NC_000015.8:g.46514105G>T	NCBI36
NG_008805.2:g.216173C>A , LRG_778:g.216173C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6594C>A	ENSP00000453958.2:p.Pro2198=
ENST00000674301.2:c.6594C>A	ENSP00000501333.2:p.Pro2198=
ENST00000682170.1:n.203C>A
ENST00000316623.10:c.6594C>A MANE Select	ENSP00000325527.5:p.Pro2198=
ENST00000674301.1:c.1593C>A	ENSP00000501333.1:p.Pro531=
ENST00000316623.9:c.6594C>A	ENSP00000325527.5:p.Pro2198=
ENST00000537463.6:c.*2357C>A	ENSP00000440294.2:n.*2357C>A
ENST00000559133.5:c.1901C>A
NM_000138.4:c.6594C>A , LRG_778t1:c.6594C>A	NP_000129.3:p.Pro2198=
NM_000138.5:c.6594C>A MANE Select	NP_000129.3:p.Pro2198=