Canonical Allele Identifier: CA360755394

Gene: FBN2

Linked Data

• MyVariant Identifiers: chr5:g.127668711T>A (hg19) ; chr5:g.128333019T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333019T>A , CM000667.2:g.128333019T>A	GRCh38
NC_000005.9:g.127668711T>A , CM000667.1:g.127668711T>A	GRCh37
NC_000005.8:g.127696610T>A	NCBI36
NG_008750.1:g.210025A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.899A>T
ENST00000703785.1:n.980A>T
ENST00000262464.9:c.4115A>T MANE Select	ENSP00000262464.4:p.Glu1372Val
ENST00000262464.8:c.4115A>T	ENSP00000262464.4:p.Glu1372Val
ENST00000507835.5:c.665A>T	ENSP00000426839.1:p.Glu222Val
ENST00000508053.5:c.4115A>T	ENSP00000424571.1:p.Glu1372Val
ENST00000508989.5:c.4016A>T	ENSP00000425596.1:p.Glu1339Val
ENST00000619499.4:c.4112A>T	ENSP00000482132.1:p.Glu1371Val
NM_001999.3:c.4115A>T	NP_001990.2:p.Glu1372Val
XM_017009228.2:c.3962A>T	XP_016864717.1:p.Glu1321Val
NM_001999.4:c.4115A>T MANE Select	NP_001990.2:p.Glu1372Val