Canonical Allele Identifier: CA392324922

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48713758C>G (hg19) ; chr15:g.48421561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421561C>G , CM000677.2:g.48421561C>G	GRCh38
NC_000015.9:g.48713758C>G , CM000677.1:g.48713758C>G	GRCh37
NC_000015.8:g.46501050C>G	NCBI36
NG_008805.2:g.229228G>C , LRG_778:g.229228G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*504G>C	ENSP00000453958.2:n.*504G>C
ENST00000674301.2:c.*1209G>C	ENSP00000501333.2:n.*1209G>C
ENST00000682170.1:n.1877G>C
ENST00000682767.1:n.993G>C
ENST00000316623.10:c.7696G>C MANE Select	ENSP00000325527.5:p.Glu2566Gln
ENST00000674301.1:c.2862G>C	ENSP00000501333.1:n.2862G>C
ENST00000316623.9:c.7696G>C	ENSP00000325527.5:p.Glu2566Gln
ENST00000559133.5:c.3065G>C
NM_000138.4:c.7696G>C , LRG_778t1:c.7696G>C	NP_000129.3:p.Glu2566Gln
NM_000138.5:c.7696G>C MANE Select	NP_000129.3:p.Glu2566Gln