Canonical Allele Identifier: CA392318413

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48703201C>G (hg19) ; chr15:g.48411004C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411004C>G , CM000677.2:g.48411004C>G	GRCh38
NC_000015.9:g.48703201C>G , CM000677.1:g.48703201C>G	GRCh37
NC_000015.8:g.46490493C>G	NCBI36
NG_008805.2:g.239785G>C , LRG_778:g.239785G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1410G>C	ENSP00000453958.2:n.*1410G>C
ENST00000682158.1:n.1983G>C
ENST00000682170.1:n.2783G>C
ENST00000682767.1:n.1899G>C
ENST00000316623.10:c.8602G>C MANE Select	ENSP00000325527.5:p.Val2868Leu
ENST00000316623.9:c.8602G>C	ENSP00000325527.5:p.Val2868Leu
ENST00000559133.5:c.3971G>C
NM_000138.4:c.8602G>C , LRG_778t1:c.8602G>C	NP_000129.3:p.Val2868Leu
NM_000138.5:c.8602G>C MANE Select	NP_000129.3:p.Val2868Leu