Canonical Allele Identifier: CA490026017

Gene: FBN1

Linked Data

• gnomAD v4: 15-48463960-G-A
• MyVariant Identifiers: chr15:g.48756157G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48463960G>A , CM000677.2:g.48463960G>A	GRCh38
NC_000015.9:g.48756157G>A , CM000677.1:g.48756157G>A	GRCh37
NC_000015.8:g.46543449G>A	NCBI36
NG_008805.2:g.186829C>T , LRG_778:g.186829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5004C>T	ENSP00000453958.2:p.Gly1668=
ENST00000674301.2:c.5004C>T	ENSP00000501333.2:p.Gly1668=
ENST00000684448.1:n.3678C>T
ENST00000316623.10:c.5004C>T MANE Select	ENSP00000325527.5:p.Gly1668=
ENST00000674301.1:c.3C>T	ENSP00000501333.1:p.Gly1=
ENST00000316623.9:c.5004C>T	ENSP00000325527.5:p.Gly1668=
ENST00000537463.6:c.*767C>T	ENSP00000440294.2:n.*767C>T
ENST00000559133.5:c.311C>T
NM_000138.4:c.5004C>T , LRG_778t1:c.5004C>T	NP_000129.3:p.Gly1668=
NM_000138.5:c.5004C>T MANE Select	NP_000129.3:p.Gly1668=