Canonical Allele Identifier: CA713391580

Gene: FBN1

Linked Data

• dbSNP Id: rs1313234034
• gnomAD v3: 15-48428163-T-A
• gnomAD v4: 15-48428163-T-A
• MyVariant Identifiers: chr15:g.48720360T>A (hg19) ; chr15:g.48428163T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428163T>A , CM000677.2:g.48428163T>A	GRCh38
NC_000015.9:g.48720360T>A , CM000677.1:g.48720360T>A	GRCh37
NC_000015.8:g.46507652T>A	NCBI36
NG_008805.2:g.222626A>T , LRG_778:g.222626A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.6997+183A>T	ENSP00000453958.2:n.6997+183A>T
ENST00000674301.2:c.*448+183A>T	ENSP00000501333.2:n.*448+183A>T
ENST00000682170.1:n.789A>T
ENST00000682767.1:n.232+183A>T
ENST00000316623.10:c.6997+183A>T MANE Select	ENSP00000325527.5:n.6997+183A>T
ENST00000674301.1:c.2101+183A>T	ENSP00000501333.1:n.2101+183A>T
ENST00000316623.9:c.6997+183A>T	ENSP00000325527.5:n.6997+183A>T
ENST00000559133.5:c.2304+183A>T
ENST00000560720.1:n.467A>T
NM_000138.4:c.6997+183A>T , LRG_778t1:c.6997+183A>T	NP_000129.3:n.6997+183A>T
NM_000138.5:c.6997+183A>T MANE Select	NP_000129.3:n.6997+183A>T