Canonical Allele Identifier: CA392322467

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48707733C>G (hg19) ; chr15:g.48415536C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48415536C>G , CM000677.2:g.48415536C>G	GRCh38
NC_000015.9:g.48707733C>G , CM000677.1:g.48707733C>G	GRCh37
NC_000015.8:g.46495025C>G	NCBI36
NG_008805.2:g.235253G>C , LRG_778:g.235253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*859G>C	ENSP00000453958.2:n.*859G>C
ENST00000674301.2:c.*1564G>C	ENSP00000501333.2:n.*1564G>C
ENST00000682158.1:n.1432G>C
ENST00000682170.1:n.2232G>C
ENST00000682767.1:n.1348G>C
ENST00000316623.10:c.8051G>C MANE Select	ENSP00000325527.5:p.Gly2684Ala
ENST00000674301.1:c.3217G>C	ENSP00000501333.1:n.3217G>C
ENST00000316623.9:c.8051G>C	ENSP00000325527.5:p.Gly2684Ala
ENST00000559133.5:c.3420G>C
ENST00000561429.1:n.306G>C
NM_000138.4:c.8051G>C , LRG_778t1:c.8051G>C	NP_000129.3:p.Gly2684Ala
NM_000138.5:c.8051G>C MANE Select	NP_000129.3:p.Gly2684Ala