Canonical Allele Identifier: CA1581270759

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338111A= , CM000667.2:g.128338111A=	GRCh38
NC_000005.9:g.127673803A= , CM000667.1:g.127673803A=	GRCh37
NC_000005.8:g.127701702A=	NCBI36
NG_008750.1:g.204933T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.268T=
ENST00000703785.1:n.349T=
ENST00000262464.9:c.3484T= MANE Select	ENSP00000262464.4:p.Cys1162=
ENST00000262464.8:c.3484T=	ENSP00000262464.4:p.Cys1162=
ENST00000507835.5:c.34T=	ENSP00000426839.1:p.Cys12=
ENST00000508053.5:c.3484T=	ENSP00000424571.1:p.Cys1162=
ENST00000508989.5:c.3385T=	ENSP00000425596.1:p.Cys1129=
ENST00000619499.4:c.3481T=	ENSP00000482132.1:p.Cys1161=
NM_001999.3:c.3484T=	NP_001990.2:p.Cys1162=
XM_017009228.2:c.3331T=	XP_016864717.1:p.Cys1111=
NM_001999.4:c.3484T= MANE Select	NP_001990.2:p.Cys1162=