Canonical Allele Identifier: CA2628330600

Gene: FBN1

Linked Data

• gnomAD v4: 15-48427468-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48427468C>A , CM000677.2:g.48427468C>A	GRCh38
NC_000015.9:g.48719665C>A , CM000677.1:g.48719665C>A	GRCh37
NC_000015.8:g.46506957C>A	NCBI36
NG_008805.2:g.223321G>T , LRG_778:g.223321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559133.6:c.*12+99G>T	ENSP00000453958.2:n.*12+99G>T
ENST00000674301.2:c.*717+99G>T	ENSP00000501333.2:n.*717+99G>T
ENST00000682170.1:n.1385+99G>T
ENST00000682767.1:n.501+99G>T
ENST00000316623.10:c.7204+99G>T MANE Select	ENSP00000325527.5:n.7204+99G>T
ENST00000674301.1:c.2370+99G>T	ENSP00000501333.1:n.2370+99G>T
ENST00000316623.9:c.7204+99G>T	ENSP00000325527.5:n.7204+99G>T
ENST00000559133.5:c.2573+99G>T
NM_000138.4:c.7204+99G>T , LRG_778t1:c.7204+99G>T	NP_000129.3:n.7204+99G>T
NM_000138.5:c.7204+99G>T MANE Select	NP_000129.3:n.7204+99G>T