Canonical Allele Identifier: CA392318817

Gene: FBN1

Linked Data

• dbSNP Id: rs2042857890
• MyVariant Identifiers: chr15:g.48703314T>C (hg19) ; chr15:g.48411117T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411117T>C , CM000677.2:g.48411117T>C	GRCh38
NC_000015.9:g.48703314T>C , CM000677.1:g.48703314T>C	GRCh37
NC_000015.8:g.46490606T>C	NCBI36
NG_008805.2:g.239672A>G , LRG_778:g.239672A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1297A>G	ENSP00000453958.2:n.*1297A>G
ENST00000674301.2:c.*2002A>G	ENSP00000501333.2:n.*2002A>G
ENST00000682158.1:n.1870A>G
ENST00000682170.1:n.2670A>G
ENST00000682767.1:n.1786A>G
ENST00000316623.10:c.8489A>G MANE Select	ENSP00000325527.5:p.Gln2830Arg
ENST00000674301.1:c.3655A>G	ENSP00000501333.1:n.3655A>G
ENST00000316623.9:c.8489A>G	ENSP00000325527.5:p.Gln2830Arg
ENST00000559133.5:c.3858A>G
NM_000138.4:c.8489A>G , LRG_778t1:c.8489A>G	NP_000129.3:p.Gln2830Arg
NM_000138.5:c.8489A>G MANE Select	NP_000129.3:p.Gln2830Arg