Canonical Allele Identifier: CA1581267352

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330621G= , CM000667.2:g.128330621G=	GRCh38
NC_000005.9:g.127666313G= , CM000667.1:g.127666313G=	GRCh37
NC_000005.8:g.127694212G=	NCBI36
NG_008750.1:g.212423C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1081C=
ENST00000703785.1:n.1162C=
ENST00000262464.9:c.4297C= MANE Select	ENSP00000262464.4:p.Arg1433=
ENST00000262464.8:c.4297C=	ENSP00000262464.4:p.Arg1433=
ENST00000507835.5:c.847C=	ENSP00000426839.1:p.Arg283=
ENST00000508053.5:c.4297C=	ENSP00000424571.1:p.Arg1433=
ENST00000508989.5:c.4198C=	ENSP00000425596.1:p.Arg1400=
ENST00000619499.4:c.4294C=	ENSP00000482132.1:p.Arg1432=
NM_001999.3:c.4297C=	NP_001990.2:p.Arg1433=
XM_017009228.2:c.4144C=	XP_016864717.1:p.Arg1382=
NM_001999.4:c.4297C= MANE Select	NP_001990.2:p.Arg1433=