Canonical Allele Identifier: CA392330800

Gene: FBN1

Linked Data

• ClinVar Variation Id: 457256
• ClinVar RCV Id: RCV000528000
• dbSNP Id: rs1555394634
• MyVariant Identifiers: chr15:g.48720634A>C (hg19) ; chr15:g.48428437A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428437A>C , CM000677.2:g.48428437A>C	GRCh38
NC_000015.9:g.48720634A>C , CM000677.1:g.48720634A>C	GRCh37
NC_000015.8:g.46507926A>C	NCBI36
NG_008805.2:g.222352T>G , LRG_778:g.222352T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6906T>G	ENSP00000453958.2:p.Cys2302Trp
ENST00000674301.2:c.*357T>G	ENSP00000501333.2:n.*357T>G
ENST00000682170.1:n.515T>G
ENST00000682767.1:n.141T>G
ENST00000316623.10:c.6906T>G MANE Select	ENSP00000325527.5:p.Cys2302Trp
ENST00000674301.1:c.2010T>G	ENSP00000501333.1:n.2010T>G
ENST00000316623.9:c.6906T>G	ENSP00000325527.5:p.Cys2302Trp
ENST00000559133.5:c.2213T>G
ENST00000560720.1:n.193T>G
NM_000138.4:c.6906T>G , LRG_778t1:c.6906T>G	NP_000129.3:p.Cys2302Trp
NM_000138.5:c.6906T>G MANE Select	NP_000129.3:p.Cys2302Trp