Canonical Allele Identifier: CA392333334

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2689053
• ClinVar RCV Id: RCV003490767
• MyVariant Identifiers: chr15:g.48725096A>G (hg19) ; chr15:g.48432899A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432899A>G , CM000677.2:g.48432899A>G	GRCh38
NC_000015.9:g.48725096A>G , CM000677.1:g.48725096A>G	GRCh37
NC_000015.8:g.46512388A>G	NCBI36
NG_008805.2:g.217890T>C , LRG_778:g.217890T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6706T>C	ENSP00000453958.2:p.Tyr2236His
ENST00000674301.2:c.*157T>C	ENSP00000501333.2:n.*157T>C
ENST00000682170.1:n.315T>C
ENST00000316623.10:c.6706T>C MANE Select	ENSP00000325527.5:p.Tyr2236His
ENST00000674301.1:c.1810T>C	ENSP00000501333.1:n.1810T>C
ENST00000316623.9:c.6706T>C	ENSP00000325527.5:p.Tyr2236His
ENST00000537463.6:c.*2469T>C	ENSP00000440294.2:n.*2469T>C
ENST00000559133.5:c.2013T>C
NM_000138.4:c.6706T>C , LRG_778t1:c.6706T>C	NP_000129.3:p.Tyr2236His
NM_000138.5:c.6706T>C MANE Select	NP_000129.3:p.Tyr2236His