Canonical Allele Identifier: CA269523649

Gene: FBN1

Linked Data

• ClinVar Variation Id: 439708
• ClinVar RCV Id: RCV000507361 ; RCV002245992 ; RCV000806890
• dbSNP Id: rs113543334
• MyVariant Identifiers: chr15:g.48725141A>G (hg19) ; chr15:g.48432944A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48432944A>G , CM000677.2:g.48432944A>G	GRCh38
NC_000015.9:g.48725141A>G , CM000677.1:g.48725141A>G	GRCh37
NC_000015.8:g.46512433A>G	NCBI36
NG_008805.2:g.217845T>C , LRG_778:g.217845T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6661T>C	ENSP00000453958.2:p.Cys2221Arg
ENST00000674301.2:c.*112T>C	ENSP00000501333.2:n.*112T>C
ENST00000682170.1:n.270T>C
ENST00000316623.10:c.6661T>C MANE Select	ENSP00000325527.5:p.Cys2221Arg
ENST00000674301.1:c.1765T>C	ENSP00000501333.1:n.1765T>C
ENST00000316623.9:c.6661T>C	ENSP00000325527.5:p.Cys2221Arg
ENST00000537463.6:c.*2424T>C	ENSP00000440294.2:n.*2424T>C
ENST00000559133.5:c.1968T>C
NM_000138.4:c.6661T>C , LRG_778t1:c.6661T>C	NP_000129.3:p.Cys2221Arg
NM_000138.5:c.6661T>C MANE Select	NP_000129.3:p.Cys2221Arg