Canonical Allele Identifier: CA360754762

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668631A>T (hg19) ; chr5:g.128332939A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332939A>T , CM000667.2:g.128332939A>T	GRCh38
NC_000005.9:g.127668631A>T , CM000667.1:g.127668631A>T	GRCh37
NC_000005.8:g.127696530A>T	NCBI36
NG_008750.1:g.210105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.979T>A
ENST00000703785.1:n.1060T>A
ENST00000262464.9:c.4195T>A MANE Select	ENSP00000262464.4:p.Trp1399Arg
ENST00000262464.8:c.4195T>A	ENSP00000262464.4:p.Trp1399Arg
ENST00000507835.5:c.745T>A	ENSP00000426839.1:p.Trp249Arg
ENST00000508053.5:c.4195T>A	ENSP00000424571.1:p.Trp1399Arg
ENST00000508989.5:c.4096T>A	ENSP00000425596.1:p.Trp1366Arg
ENST00000619499.4:c.4192T>A	ENSP00000482132.1:p.Trp1398Arg
NM_001999.3:c.4195T>A	NP_001990.2:p.Trp1399Arg
XM_017009228.2:c.4042T>A	XP_016864717.1:p.Trp1348Arg
NM_001999.4:c.4195T>A MANE Select	NP_001990.2:p.Trp1399Arg