Canonical Allele Identifier: CA392332030

Gene: FBN1

Linked Data

• ClinVar Variation Id: 1325483
• ClinVar RCV Id: RCV002246095
• dbSNP Id: rs2141303537
• MyVariant Identifiers: chr15:g.48787338A>G (hg19) ; chr15:g.48495141A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48495141A>G , CM000677.2:g.48495141A>G	GRCh38
NC_000015.9:g.48787338A>G , CM000677.1:g.48787338A>G	GRCh37
NC_000015.8:g.46574630A>G	NCBI36
NG_008805.2:g.155648T>C , LRG_778:g.155648T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.2659T>C	ENSP00000453958.2:p.Cys887Arg
ENST00000674301.2:c.2659T>C	ENSP00000501333.2:p.Cys887Arg
ENST00000684448.1:n.1333T>C
ENST00000316623.10:c.2659T>C MANE Select	ENSP00000325527.5:p.Cys887Arg
ENST00000316623.9:c.2659T>C	ENSP00000325527.5:p.Cys887Arg
ENST00000537463.6:c.637-20491T>C	ENSP00000440294.2:n.637-20491T>C
NM_000138.4:c.2659T>C , LRG_778t1:c.2659T>C	NP_000129.3:p.Cys887Arg
NM_000138.5:c.2659T>C MANE Select	NP_000129.3:p.Cys887Arg