Canonical Allele Identifier: CA2675121723

Gene: FBN2

Linked Data

• gnomAD v4: 5-128527861-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128527863_128527864del , CM000667.2:g.128527863_128527864del	GRCh38
NC_000005.9:g.127863556_127863557del , CM000667.1:g.127863556_127863557del	GRCh37
NC_000005.8:g.127891455_127891456del	NCBI36
NG_008750.1:g.15180_15181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508053.6:c.532+9_532+10del	ENSP00000424571.2:n.532+9_532+10del
ENST00000703787.1:n.239+9_239+10del
ENST00000262464.9:c.532+9_532+10del MANE Select	ENSP00000262464.4:n.532+9_532+10del
ENST00000262464.8:c.532+9_532+10del	ENSP00000262464.4:n.532+9_532+10del
ENST00000502468.5:c.532+9_532+10del	ENSP00000424753.1:n.532+9_532+10del
ENST00000508053.5:c.532+9_532+10del	ENSP00000424571.1:n.532+9_532+10del
ENST00000508989.5:c.433+9_433+10del	ENSP00000425596.1:n.433+9_433+10del
ENST00000514742.1:n.1152+9_1152+10del
ENST00000619499.4:c.532+9_532+10del	ENSP00000482132.1:n.532+9_532+10del
ENST00000620257.1:c.532+9_532+10del	ENSP00000479157.1:n.532+9_532+10del
NM_001999.3:c.532+9_532+10del	NP_001990.2:n.532+9_532+10del
XM_017009228.2:c.532+9_532+10del	XP_016864717.1:n.532+9_532+10del
NM_001999.4:c.532+9_532+10del MANE Select	NP_001990.2:n.532+9_532+10del