Canonical Allele Identifier: CA392319704

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411295-C-A
• MyVariant Identifiers: chr15:g.48703492C>A (hg19) ; chr15:g.48411295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411295C>A , CM000677.2:g.48411295C>A	GRCh38
NC_000015.9:g.48703492C>A , CM000677.1:g.48703492C>A	GRCh37
NC_000015.8:g.46490784C>A	NCBI36
NG_008805.2:g.239494G>T , LRG_778:g.239494G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1119G>T	ENSP00000453958.2:n.*1119G>T
ENST00000674301.2:c.*1824G>T	ENSP00000501333.2:n.*1824G>T
ENST00000682158.1:n.1692G>T
ENST00000682170.1:n.2492G>T
ENST00000682767.1:n.1608G>T
ENST00000316623.10:c.8311G>T MANE Select	ENSP00000325527.5:p.Val2771Phe
ENST00000674301.1:c.3477G>T	ENSP00000501333.1:n.3477G>T
ENST00000316623.9:c.8311G>T	ENSP00000325527.5:p.Val2771Phe
ENST00000559133.5:c.3680G>T
ENST00000561429.1:n.566G>T
NM_000138.4:c.8311G>T , LRG_778t1:c.8311G>T	NP_000129.3:p.Val2771Phe
NM_000138.5:c.8311G>T MANE Select	NP_000129.3:p.Val2771Phe