Canonical Allele Identifier: CA1581268384

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128332933C= , CM000667.2:g.128332933C=	GRCh38
NC_000005.9:g.127668625C= , CM000667.1:g.127668625C=	GRCh37
NC_000005.8:g.127696524C=	NCBI36
NG_008750.1:g.210111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.985G=
ENST00000703785.1:n.1066G=
ENST00000262464.9:c.4201G= MANE Select	ENSP00000262464.4:p.Gly1401=
ENST00000262464.8:c.4201G=	ENSP00000262464.4:p.Gly1401=
ENST00000507835.5:c.751G=	ENSP00000426839.1:p.Gly251=
ENST00000508053.5:c.4201G=	ENSP00000424571.1:p.Gly1401=
ENST00000508989.5:c.4102G=	ENSP00000425596.1:p.Gly1368=
ENST00000619499.4:c.4198G=	ENSP00000482132.1:p.Gly1400=
NM_001999.3:c.4201G=	NP_001990.2:p.Gly1401=
XM_017009228.2:c.4048G=	XP_016864717.1:p.Gly1350=
NM_001999.4:c.4201G= MANE Select	NP_001990.2:p.Gly1401=