Canonical Allele Identifier: CA2675116628

Gene: FBN2

Linked Data

• gnomAD v4: 5-128330713-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330713A>T , CM000667.2:g.128330713A>T	GRCh38
NC_000005.9:g.127666405A>T , CM000667.1:g.127666405A>T	GRCh37
NC_000005.8:g.127694304A>T	NCBI36
NG_008750.1:g.212331T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1007-18T>A
ENST00000703785.1:n.1088-18T>A
ENST00000262464.9:c.4223-18T>A MANE Select	ENSP00000262464.4:n.4223-18T>A
ENST00000262464.8:c.4223-18T>A	ENSP00000262464.4:n.4223-18T>A
ENST00000507835.5:c.773-18T>A	ENSP00000426839.1:n.773-18T>A
ENST00000508053.5:c.4223-18T>A	ENSP00000424571.1:n.4223-18T>A
ENST00000508989.5:c.4124-18T>A	ENSP00000425596.1:n.4124-18T>A
ENST00000619499.4:c.4220-18T>A	ENSP00000482132.1:n.4220-18T>A
NM_001999.3:c.4223-18T>A	NP_001990.2:n.4223-18T>A
XM_017009228.2:c.4070-18T>A	XP_016864717.1:n.4070-18T>A
NM_001999.4:c.4223-18T>A MANE Select	NP_001990.2:n.4223-18T>A