Canonical Allele Identifier: CA1581268381

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332927C= , CM000667.2:g.128332927C=	GRCh38
NC_000005.9:g.127668619C= , CM000667.1:g.127668619C=	GRCh37
NC_000005.8:g.127696518C=	NCBI36
NG_008750.1:g.210117G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.991G=
ENST00000703785.1:n.1072G=
ENST00000262464.9:c.4207G= MANE Select	ENSP00000262464.4:p.Gly1403=
ENST00000262464.8:c.4207G=	ENSP00000262464.4:p.Gly1403=
ENST00000507835.5:c.757G=	ENSP00000426839.1:p.Gly253=
ENST00000508053.5:c.4207G=	ENSP00000424571.1:p.Gly1403=
ENST00000508989.5:c.4108G=	ENSP00000425596.1:p.Gly1370=
ENST00000619499.4:c.4204G=	ENSP00000482132.1:p.Gly1402=
NM_001999.3:c.4207G=	NP_001990.2:p.Gly1403=
XM_017009228.2:c.4054G=	XP_016864717.1:p.Gly1352=
NM_001999.4:c.4207G= MANE Select	NP_001990.2:p.Gly1403=