Canonical Allele Identifier: CA490023028

Gene: FBN1

Linked Data

• gnomAD v4: 15-48446821-G-A
• MyVariant Identifiers: chr15:g.48739018G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48446821G>A , CM000677.2:g.48446821G>A	GRCh38
NC_000015.9:g.48739018G>A , CM000677.1:g.48739018G>A	GRCh37
NC_000015.8:g.46526310G>A	NCBI36
NG_008805.2:g.203968C>T , LRG_778:g.203968C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5673C>T	ENSP00000453958.2:p.Asp1891=
ENST00000674301.2:c.5673C>T	ENSP00000501333.2:p.Asp1891=
ENST00000684448.1:n.4347C>T
ENST00000316623.10:c.5673C>T MANE Select	ENSP00000325527.5:p.Asp1891=
ENST00000674301.1:c.672C>T	ENSP00000501333.1:p.Asp224=
ENST00000316623.9:c.5673C>T	ENSP00000325527.5:p.Asp1891=
ENST00000537463.6:c.*1436C>T	ENSP00000440294.2:n.*1436C>T
ENST00000559133.5:c.980C>T
NM_000138.4:c.5673C>T , LRG_778t1:c.5673C>T	NP_000129.3:p.Asp1891=
NM_000138.5:c.5673C>T MANE Select	NP_000129.3:p.Asp1891=