Canonical Allele Identifier: CA392330570

Gene: FBN1

Linked Data

• ClinVar Variation Id: 527165
• ClinVar RCV Id: RCV000631944 ; RCV002477386
• dbSNP Id: rs794728261
• gnomAD v4: 15-48428384-T-C
• MyVariant Identifiers: chr15:g.48720581T>C (hg19) ; chr15:g.48428384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428384T>C , CM000677.2:g.48428384T>C	GRCh38
NC_000015.9:g.48720581T>C , CM000677.1:g.48720581T>C	GRCh37
NC_000015.8:g.46507873T>C	NCBI36
NG_008805.2:g.222405A>G , LRG_778:g.222405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6959A>G	ENSP00000453958.2:p.Asp2320Gly
ENST00000674301.2:c.*410A>G	ENSP00000501333.2:n.*410A>G
ENST00000682170.1:n.568A>G
ENST00000682767.1:n.194A>G
ENST00000316623.10:c.6959A>G MANE Select	ENSP00000325527.5:p.Asp2320Gly
ENST00000674301.1:c.2063A>G	ENSP00000501333.1:n.2063A>G
ENST00000316623.9:c.6959A>G	ENSP00000325527.5:p.Asp2320Gly
ENST00000559133.5:c.2266A>G
ENST00000560720.1:n.246A>G
NM_000138.4:c.6959A>G , LRG_778t1:c.6959A>G	NP_000129.3:p.Asp2320Gly
NM_000138.5:c.6959A>G MANE Select	NP_000129.3:p.Asp2320Gly