Canonical Allele Identifier: CA392340272

Gene: FBN1

Linked Data

• ClinVar Variation Id: 527199
• ClinVar RCV Id: RCV000631995 ; RCV001190262 ; RCV002483785
• dbSNP Id: rs1555395768
• gnomAD v4: 15-48445502-C-T
• MyVariant Identifiers: chr15:g.48737699C>T (hg19) ; chr15:g.48445502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445502C>T , CM000677.2:g.48445502C>T	GRCh38
NC_000015.9:g.48737699C>T , CM000677.1:g.48737699C>T	GRCh37
NC_000015.8:g.46524991C>T	NCBI36
NG_008805.2:g.205287G>A , LRG_778:g.205287G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5791G>A	ENSP00000453958.2:p.Val1931Ile
ENST00000674301.2:c.5791G>A	ENSP00000501333.2:p.Val1931Ile
ENST00000684448.1:n.4465G>A
ENST00000316623.10:c.5791G>A MANE Select	ENSP00000325527.5:p.Val1931Ile
ENST00000674301.1:c.790G>A	ENSP00000501333.1:p.Val264Ile
ENST00000316623.9:c.5791G>A	ENSP00000325527.5:p.Val1931Ile
ENST00000537463.6:c.*1554G>A	ENSP00000440294.2:n.*1554G>A
ENST00000559133.5:c.1098G>A
NM_000138.4:c.5791G>A , LRG_778t1:c.5791G>A	NP_000129.3:p.Val1931Ile
NM_000138.5:c.5791G>A MANE Select	NP_000129.3:p.Val1931Ile