Canonical Allele Identifier: CA2730866111

Gene: FBN1

Linked Data

• dbSNP Id: rs2141229530

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428080T>G , CM000677.2:g.48428080T>G	GRCh38
NC_000015.9:g.48720277T>G , CM000677.1:g.48720277T>G	GRCh37
NC_000015.8:g.46507569T>G	NCBI36
NG_008805.2:g.222709A>C , LRG_778:g.222709A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6998-137A>C	ENSP00000453958.2:n.6998-137A>C
ENST00000674301.2:c.*449-137A>C	ENSP00000501333.2:n.*449-137A>C
ENST00000682170.1:n.872A>C
ENST00000682767.1:n.233-137A>C
ENST00000316623.10:c.6997+266A>C MANE Select	ENSP00000325527.5:n.6997+266A>C
ENST00000674301.1:c.2102-137A>C	ENSP00000501333.1:n.2102-137A>C
ENST00000316623.9:c.6997+266A>C	ENSP00000325527.5:n.6997+266A>C
ENST00000559133.5:c.2305-137A>C
ENST00000560720.1:n.550A>C
NM_000138.4:c.6997+266A>C , LRG_778t1:c.6997+266A>C	NP_000129.3:n.6997+266A>C
NM_000138.5:c.6997+266A>C MANE Select	NP_000129.3:n.6997+266A>C