Canonical Allele Identifier: CA2628331621

Gene: FBN1

Linked Data

• gnomAD v4: 15-48428325-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48428325T>C , CM000677.2:g.48428325T>C	GRCh38
NC_000015.9:g.48720522T>C , CM000677.1:g.48720522T>C	GRCh37
NC_000015.8:g.46507814T>C	NCBI36
NG_008805.2:g.222464A>G , LRG_778:g.222464A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.6997+21A>G	ENSP00000453958.2:n.6997+21A>G
ENST00000674301.2:c.*448+21A>G	ENSP00000501333.2:n.*448+21A>G
ENST00000682170.1:n.627A>G
ENST00000682767.1:n.232+21A>G
ENST00000316623.10:c.6997+21A>G MANE Select	ENSP00000325527.5:n.6997+21A>G
ENST00000674301.1:c.2101+21A>G	ENSP00000501333.1:n.2101+21A>G
ENST00000316623.9:c.6997+21A>G	ENSP00000325527.5:n.6997+21A>G
ENST00000559133.5:c.2304+21A>G
ENST00000560720.1:n.305A>G
NM_000138.4:c.6997+21A>G , LRG_778t1:c.6997+21A>G	NP_000129.3:n.6997+21A>G
NM_000138.5:c.6997+21A>G MANE Select	NP_000129.3:n.6997+21A>G