Canonical Allele Identifier: CA1581271289

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128339184T= , CM000667.2:g.128339184T=	GRCh38
NC_000005.9:g.127674876T= , CM000667.1:g.127674876T=	GRCh37
NC_000005.8:g.127702775T=	NCBI36
NG_008750.1:g.203860A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.5A=
ENST00000703785.1:n.86A=
ENST00000262464.9:c.3344-123A= MANE Select	ENSP00000262464.4:n.3344-123A=
ENST00000262464.8:c.3344-123A=	ENSP00000262464.4:n.3344-123A=
ENST00000507835.5:c.-230A=	ENSP00000426839.1:n.-230A=
ENST00000508053.5:c.3344-123A=	ENSP00000424571.1:n.3344-123A=
ENST00000508989.5:c.3245-123A=	ENSP00000425596.1:n.3245-123A=
ENST00000619499.4:c.3341-123A=	ENSP00000482132.1:n.3341-123A=
NM_001999.3:c.3344-123A=	NP_001990.2:n.3344-123A=
XM_017009228.2:c.3191-123A=	XP_016864717.1:n.3191-123A=
NM_001999.4:c.3344-123A= MANE Select	NP_001990.2:n.3344-123A=