Canonical Allele Identifier: CA059866

Gene: FBN1

Linked Data

• ClinVar Variation Id: 377863
• ClinVar RCV Id: RCV000428763 ; RCV000457337 ; RCV001179775 ; RCV000659585 ; RCV001579696 ; RCV003995960
• dbSNP Id: rs376119827
• ExAC: 15:48703571 C / T
• gnomAD v2: 15-48703571-C-T
• gnomAD v3: 15-48411374-C-T
• gnomAD v4: 15-48411374-C-T
• MyVariant Identifiers: chr15:g.48703571C>T (hg19) ; chr15:g.48411374C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411374C>T , CM000677.2:g.48411374C>T	GRCh38
NC_000015.9:g.48703571C>T , CM000677.1:g.48703571C>T	GRCh37
NC_000015.8:g.46490863C>T	NCBI36
NG_008805.2:g.239415G>A , LRG_778:g.239415G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1040G>A	ENSP00000453958.2:n.*1040G>A
ENST00000674301.2:c.*1745G>A	ENSP00000501333.2:n.*1745G>A
ENST00000682158.1:n.1613G>A
ENST00000682170.1:n.2413G>A
ENST00000682767.1:n.1529G>A
ENST00000316623.10:c.8232G>A MANE Select	ENSP00000325527.5:p.Gln2744=
ENST00000674301.1:c.3398G>A	ENSP00000501333.1:n.3398G>A
ENST00000316623.9:c.8232G>A	ENSP00000325527.5:p.Gln2744=
ENST00000559133.5:c.3601G>A
ENST00000561429.1:n.487G>A
NM_000138.4:c.8232G>A , LRG_778t1:c.8232G>A	NP_000129.3:p.Gln2744=
NM_000138.5:c.8232G>A MANE Select	NP_000129.3:p.Gln2744=