Canonical Allele Identifier: CA1581267311

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330526T= , CM000667.2:g.128330526T=	GRCh38
NC_000005.9:g.127666218T= , CM000667.1:g.127666218T=	GRCh37
NC_000005.8:g.127694117T=	NCBI36
NG_008750.1:g.212518A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1129+47A=
ENST00000703785.1:n.1210+47A=
ENST00000262464.9:c.4345+47A= MANE Select	ENSP00000262464.4:n.4345+47A=
ENST00000262464.8:c.4345+47A=	ENSP00000262464.4:n.4345+47A=
ENST00000507835.5:c.895+47A=	ENSP00000426839.1:n.895+47A=
ENST00000508053.5:c.4345+47A=	ENSP00000424571.1:n.4345+47A=
ENST00000508989.5:c.4246+47A=	ENSP00000425596.1:n.4246+47A=
ENST00000619499.4:c.4342+47A=	ENSP00000482132.1:n.4342+47A=
NM_001999.3:c.4345+47A=	NP_001990.2:n.4345+47A=
XM_017009228.2:c.4192+47A=	XP_016864717.1:n.4192+47A=
NM_001999.4:c.4345+47A= MANE Select	NP_001990.2:n.4345+47A=