Canonical Allele Identifier: CA392319051

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703364G>T (hg19) ; chr15:g.48411167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411167G>T , CM000677.2:g.48411167G>T	GRCh38
NC_000015.9:g.48703364G>T , CM000677.1:g.48703364G>T	GRCh37
NC_000015.8:g.46490656G>T	NCBI36
NG_008805.2:g.239622C>A , LRG_778:g.239622C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1247C>A	ENSP00000453958.2:n.*1247C>A
ENST00000674301.2:c.*1952C>A	ENSP00000501333.2:n.*1952C>A
ENST00000682158.1:n.1820C>A
ENST00000682170.1:n.2620C>A
ENST00000682767.1:n.1736C>A
ENST00000316623.10:c.8439C>A MANE Select	ENSP00000325527.5:p.Ser2813Arg
ENST00000674301.1:c.3605C>A	ENSP00000501333.1:n.3605C>A
ENST00000316623.9:c.8439C>A	ENSP00000325527.5:p.Ser2813Arg
ENST00000559133.5:c.3808C>A
NM_000138.4:c.8439C>A , LRG_778t1:c.8439C>A	NP_000129.3:p.Ser2813Arg
NM_000138.5:c.8439C>A MANE Select	NP_000129.3:p.Ser2813Arg