Canonical Allele Identifier: CA490017794

Gene: FBN1

Linked Data

• gnomAD v4: 15-48428365-G-T
• MyVariant Identifiers: chr15:g.48720562G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428365G>T , CM000677.2:g.48428365G>T	GRCh38
NC_000015.9:g.48720562G>T , CM000677.1:g.48720562G>T	GRCh37
NC_000015.8:g.46507854G>T	NCBI36
NG_008805.2:g.222424C>A , LRG_778:g.222424C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6978C>A	ENSP00000453958.2:p.Pro2326=
ENST00000674301.2:c.*429C>A	ENSP00000501333.2:n.*429C>A
ENST00000682170.1:n.587C>A
ENST00000682767.1:n.213C>A
ENST00000316623.10:c.6978C>A MANE Select	ENSP00000325527.5:p.Pro2326=
ENST00000674301.1:c.2082C>A	ENSP00000501333.1:n.2082C>A
ENST00000316623.9:c.6978C>A	ENSP00000325527.5:p.Pro2326=
ENST00000559133.5:c.2285C>A
ENST00000560720.1:n.265C>A
NM_000138.4:c.6978C>A , LRG_778t1:c.6978C>A	NP_000129.3:p.Pro2326=
NM_000138.5:c.6978C>A MANE Select	NP_000129.3:p.Pro2326=