Canonical Allele Identifier: CA392323447

Gene: FBN1

Linked Data

• ClinVar Variation Id: 523335
• ClinVar RCV Id: RCV000626618
• dbSNP Id: rs1555393889
• MyVariant Identifiers: chr15:g.48707955T>C (hg19) ; chr15:g.48415758T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415758T>C , CM000677.2:g.48415758T>C	GRCh38
NC_000015.9:g.48707955T>C , CM000677.1:g.48707955T>C	GRCh37
NC_000015.8:g.46495247T>C	NCBI36
NG_008805.2:g.235031A>G , LRG_778:g.235031A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*637A>G	ENSP00000453958.2:n.*637A>G
ENST00000674301.2:c.*1342A>G	ENSP00000501333.2:n.*1342A>G
ENST00000682158.1:n.1210A>G
ENST00000682170.1:n.2010A>G
ENST00000682767.1:n.1126A>G
ENST00000316623.10:c.7829A>G MANE Select	ENSP00000325527.5:p.Glu2610Gly
ENST00000674301.1:c.2995A>G	ENSP00000501333.1:n.2995A>G
ENST00000316623.9:c.7829A>G	ENSP00000325527.5:p.Glu2610Gly
ENST00000559133.5:c.3198A>G
ENST00000561429.1:n.84A>G
NM_000138.4:c.7829A>G , LRG_778t1:c.7829A>G	NP_000129.3:p.Glu2610Gly
NM_000138.5:c.7829A>G MANE Select	NP_000129.3:p.Glu2610Gly