Canonical Allele Identifier: CA2740096636

Gene: FBN1

Linked Data

• ClinVar Variation Id: 2953213
• ClinVar RCV Id: RCV003810331

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48445515A>C , CM000677.2:g.48445515A>C	GRCh38
NC_000015.9:g.48737712A>C , CM000677.1:g.48737712A>C	GRCh37
NC_000015.8:g.46525004A>C	NCBI36
NG_008805.2:g.205274T>G , LRG_778:g.205274T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.5789-11T>G	ENSP00000453958.2:n.5789-11T>G
ENST00000674301.2:c.5789-11T>G	ENSP00000501333.2:n.5789-11T>G
ENST00000684448.1:n.4463-11T>G
ENST00000316623.10:c.5789-11T>G MANE Select	ENSP00000325527.5:n.5789-11T>G
ENST00000674301.1:c.788-11T>G	ENSP00000501333.1:n.788-11T>G
ENST00000316623.9:c.5789-11T>G	ENSP00000325527.5:n.5789-11T>G
ENST00000537463.6:c.*1552-11T>G	ENSP00000440294.2:n.*1552-11T>G
ENST00000559133.5:c.1096-11T>G
NM_000138.4:c.5789-11T>G , LRG_778t1:c.5789-11T>G	NP_000129.3:n.5789-11T>G
NM_000138.5:c.5789-11T>G MANE Select	NP_000129.3:n.5789-11T>G