Canonical Allele Identifier: CA490118993

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703475T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411278T>C , CM000677.2:g.48411278T>C	GRCh38
NC_000015.9:g.48703475T>C , CM000677.1:g.48703475T>C	GRCh37
NC_000015.8:g.46490767T>C	NCBI36
NG_008805.2:g.239511A>G , LRG_778:g.239511A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1136A>G	ENSP00000453958.2:n.*1136A>G
ENST00000674301.2:c.*1841A>G	ENSP00000501333.2:n.*1841A>G
ENST00000682158.1:n.1709A>G
ENST00000682170.1:n.2509A>G
ENST00000682767.1:n.1625A>G
ENST00000316623.10:c.8328A>G MANE Select	ENSP00000325527.5:p.Arg2776=
ENST00000674301.1:c.3494A>G	ENSP00000501333.1:n.3494A>G
ENST00000316623.9:c.8328A>G	ENSP00000325527.5:p.Arg2776=
ENST00000559133.5:c.3697A>G
ENST00000561429.1:n.583A>G
NM_000138.4:c.8328A>G , LRG_778t1:c.8328A>G	NP_000129.3:p.Arg2776=
NM_000138.5:c.8328A>G MANE Select	NP_000129.3:p.Arg2776=