Canonical Allele Identifier: CA059614

Gene: FBN1

Linked Data

• dbSNP Id: rs367809284
• ExAC: 15:48704908 C / T
• gnomAD v2: 15-48704908-C-T
• MyVariant Identifiers: chr15:g.48704908C>T (hg19) ; chr15:g.48412711C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48412711C>T , CM000677.2:g.48412711C>T	GRCh38
NC_000015.9:g.48704908C>T , CM000677.1:g.48704908C>T	GRCh37
NC_000015.8:g.46492200C>T	NCBI36
NG_008805.2:g.238078G>A , LRG_778:g.238078G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*892G>A	ENSP00000453958.2:n.*892G>A
ENST00000674301.2:c.*1597G>A	ENSP00000501333.2:n.*1597G>A
ENST00000682158.1:n.1465G>A
ENST00000682170.1:n.2265G>A
ENST00000682767.1:n.1381G>A
ENST00000316623.10:c.8084G>A MANE Select	ENSP00000325527.5:p.Gly2695Glu
ENST00000674301.1:c.3250G>A	ENSP00000501333.1:n.3250G>A
ENST00000316623.9:c.8084G>A	ENSP00000325527.5:p.Gly2695Glu
ENST00000559133.5:c.3453G>A
ENST00000561429.1:n.339G>A
NM_000138.4:c.8084G>A , LRG_778t1:c.8084G>A	NP_000129.3:p.Gly2695Glu
NM_000138.5:c.8084G>A MANE Select	NP_000129.3:p.Gly2695Glu