Canonical Allele Identifier: CA490119040

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411356-A-G
• MyVariant Identifiers: chr15:g.48703553A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411356A>G , CM000677.2:g.48411356A>G	GRCh38
NC_000015.9:g.48703553A>G , CM000677.1:g.48703553A>G	GRCh37
NC_000015.8:g.46490845A>G	NCBI36
NG_008805.2:g.239433T>C , LRG_778:g.239433T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1058T>C	ENSP00000453958.2:n.*1058T>C
ENST00000674301.2:c.*1763T>C	ENSP00000501333.2:n.*1763T>C
ENST00000682158.1:n.1631T>C
ENST00000682170.1:n.2431T>C
ENST00000682767.1:n.1547T>C
ENST00000316623.10:c.8250T>C MANE Select	ENSP00000325527.5:p.Asn2750=
ENST00000674301.1:c.3416T>C	ENSP00000501333.1:n.3416T>C
ENST00000316623.9:c.8250T>C	ENSP00000325527.5:p.Asn2750=
ENST00000559133.5:c.3619T>C
ENST00000561429.1:n.505T>C
NM_000138.4:c.8250T>C , LRG_778t1:c.8250T>C	NP_000129.3:p.Asn2750=
NM_000138.5:c.8250T>C MANE Select	NP_000129.3:p.Asn2750=