Canonical Allele Identifier: CA392319729

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411298-G-C
• MyVariant Identifiers: chr15:g.48703495G>C (hg19) ; chr15:g.48411298G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411298G>C , CM000677.2:g.48411298G>C	GRCh38
NC_000015.9:g.48703495G>C , CM000677.1:g.48703495G>C	GRCh37
NC_000015.8:g.46490787G>C	NCBI36
NG_008805.2:g.239491C>G , LRG_778:g.239491C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*1116C>G	ENSP00000453958.2:n.*1116C>G
ENST00000674301.2:c.*1821C>G	ENSP00000501333.2:n.*1821C>G
ENST00000682158.1:n.1689C>G
ENST00000682170.1:n.2489C>G
ENST00000682767.1:n.1605C>G
ENST00000316623.10:c.8308C>G MANE Select	ENSP00000325527.5:p.His2770Asp
ENST00000674301.1:c.3474C>G	ENSP00000501333.1:n.3474C>G
ENST00000316623.9:c.8308C>G	ENSP00000325527.5:p.His2770Asp
ENST00000559133.5:c.3677C>G
ENST00000561429.1:n.563C>G
NM_000138.4:c.8308C>G , LRG_778t1:c.8308C>G	NP_000129.3:p.His2770Asp
NM_000138.5:c.8308C>G MANE Select	NP_000129.3:p.His2770Asp