Canonical Allele Identifier: CA1581270757

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338106T= , CM000667.2:g.128338106T=	GRCh38
NC_000005.9:g.127673798T= , CM000667.1:g.127673798T=	GRCh37
NC_000005.8:g.127701697T=	NCBI36
NG_008750.1:g.204938A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.273A=
ENST00000703785.1:n.354A=
ENST00000262464.9:c.3489A= MANE Select	ENSP00000262464.4:p.Glu1163=
ENST00000262464.8:c.3489A=	ENSP00000262464.4:p.Glu1163=
ENST00000507835.5:c.39A=	ENSP00000426839.1:p.Glu13=
ENST00000508053.5:c.3489A=	ENSP00000424571.1:p.Glu1163=
ENST00000508989.5:c.3390A=	ENSP00000425596.1:p.Glu1130=
ENST00000619499.4:c.3486A=	ENSP00000482132.1:p.Glu1162=
NM_001999.3:c.3489A=	NP_001990.2:p.Glu1163=
XM_017009228.2:c.3336A=	XP_016864717.1:p.Glu1112=
NM_001999.4:c.3489A= MANE Select	NP_001990.2:p.Glu1163=