Canonical Allele Identifier: CA392325769

Gene: FBN1

Linked Data

• MyVariant Identifiers: chr15:g.48713865G>C (hg19) ; chr15:g.48421668G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48421668G>C , CM000677.2:g.48421668G>C	GRCh38
NC_000015.9:g.48713865G>C , CM000677.1:g.48713865G>C	GRCh37
NC_000015.8:g.46501157G>C	NCBI36
NG_008805.2:g.229121C>G , LRG_778:g.229121C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*397C>G	ENSP00000453958.2:n.*397C>G
ENST00000674301.2:c.*1102C>G	ENSP00000501333.2:n.*1102C>G
ENST00000682170.1:n.1770C>G
ENST00000682767.1:n.886C>G
ENST00000316623.10:c.7589C>G MANE Select	ENSP00000325527.5:p.Ser2530Cys
ENST00000674301.1:c.2755C>G	ENSP00000501333.1:n.2755C>G
ENST00000316623.9:c.7589C>G	ENSP00000325527.5:p.Ser2530Cys
ENST00000559133.5:c.2958C>G
NM_000138.4:c.7589C>G , LRG_778t1:c.7589C>G	NP_000129.3:p.Ser2530Cys
NM_000138.5:c.7589C>G MANE Select	NP_000129.3:p.Ser2530Cys