Canonical Allele Identifier: CA392321456

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48704885C>G (hg19) ; chr15:g.48412688C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412688C>G , CM000677.2:g.48412688C>G	GRCh38
NC_000015.9:g.48704885C>G , CM000677.1:g.48704885C>G	GRCh37
NC_000015.8:g.46492177C>G	NCBI36
NG_008805.2:g.238101G>C , LRG_778:g.238101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*915G>C	ENSP00000453958.2:n.*915G>C
ENST00000674301.2:c.*1620G>C	ENSP00000501333.2:n.*1620G>C
ENST00000682158.1:n.1488G>C
ENST00000682170.1:n.2288G>C
ENST00000682767.1:n.1404G>C
ENST00000316623.10:c.8107G>C MANE Select	ENSP00000325527.5:p.Gly2703Arg
ENST00000674301.1:c.3273G>C	ENSP00000501333.1:n.3273G>C
ENST00000316623.9:c.8107G>C	ENSP00000325527.5:p.Gly2703Arg
ENST00000559133.5:c.3476G>C
ENST00000561429.1:n.362G>C
NM_000138.4:c.8107G>C , LRG_778t1:c.8107G>C	NP_000129.3:p.Gly2703Arg
NM_000138.5:c.8107G>C MANE Select	NP_000129.3:p.Gly2703Arg