Canonical Allele Identifier: CA490024488

Gene: FBN1

Linked Data

• ClinVar Variation Id: 921080
• ClinVar RCV Id: RCV001180229
• dbSNP Id: rs2043686500
• MyVariant Identifiers: chr15:g.48796129G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48503932G>A , CM000677.2:g.48503932G>A	GRCh38
NC_000015.9:g.48796129G>A , CM000677.1:g.48796129G>A	GRCh37
NC_000015.8:g.46583421G>A	NCBI36
NG_008805.2:g.146857C>T , LRG_778:g.146857C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.1968C>T	ENSP00000453958.2:p.His656=
ENST00000674301.2:c.1968C>T	ENSP00000501333.2:p.His656=
ENST00000684448.1:n.642C>T
ENST00000316623.10:c.1968C>T MANE Select	ENSP00000325527.5:p.His656=
ENST00000316623.9:c.1968C>T	ENSP00000325527.5:p.His656=
ENST00000537463.6:c.637-29282C>T	ENSP00000440294.2:n.637-29282C>T
NM_000138.4:c.1968C>T , LRG_778t1:c.1968C>T	NP_000129.3:p.His656=
NM_000138.5:c.1968C>T MANE Select	NP_000129.3:p.His656=