Canonical Allele Identifier: CA490022713

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48737679T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445482T>A , CM000677.2:g.48445482T>A	GRCh38
NC_000015.9:g.48737679T>A , CM000677.1:g.48737679T>A	GRCh37
NC_000015.8:g.46524971T>A	NCBI36
NG_008805.2:g.205307A>T , LRG_778:g.205307A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5811A>T	ENSP00000453958.2:p.Gly1937=
ENST00000674301.2:c.5811A>T	ENSP00000501333.2:p.Gly1937=
ENST00000684448.1:n.4485A>T
ENST00000316623.10:c.5811A>T MANE Select	ENSP00000325527.5:p.Gly1937=
ENST00000674301.1:c.810A>T	ENSP00000501333.1:p.Gly270=
ENST00000316623.9:c.5811A>T	ENSP00000325527.5:p.Gly1937=
ENST00000537463.6:c.*1574A>T	ENSP00000440294.2:n.*1574A>T
ENST00000559133.5:c.1118A>T
NM_000138.4:c.5811A>T , LRG_778t1:c.5811A>T	NP_000129.3:p.Gly1937=
NM_000138.5:c.5811A>T MANE Select	NP_000129.3:p.Gly1937=