Canonical Allele Identifier: CA2675118702

Gene: FBN2

Linked Data

• gnomAD v4: 5-128357138-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128357140del , CM000667.2:g.128357140del	GRCh38
NC_000005.9:g.127692832del , CM000667.1:g.127692832del	GRCh37
NC_000005.8:g.127720731del	NCBI36
NG_008750.1:g.185905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262464.9:c.2674+137del MANE Select	ENSP00000262464.4:n.2674+137del
ENST00000262464.8:c.2674+137del	ENSP00000262464.4:n.2674+137del
ENST00000508053.5:c.2674+137del	ENSP00000424571.1:n.2674+137del
ENST00000508989.5:c.2575+137del	ENSP00000425596.1:n.2575+137del
ENST00000619499.4:c.2671+137del	ENSP00000482132.1:n.2671+137del
NM_001999.3:c.2674+137del	NP_001990.2:n.2674+137del
XM_017009228.2:c.2521+137del	XP_016864717.1:n.2521+137del
NM_001999.4:c.2674+137del MANE Select	NP_001990.2:n.2674+137del