Canonical Allele Identifier: CA1581267361

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330635G= , CM000667.2:g.128330635G=	GRCh38
NC_000005.9:g.127666327G= , CM000667.1:g.127666327G=	GRCh37
NC_000005.8:g.127694226G=	NCBI36
NG_008750.1:g.212409C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1067C=
ENST00000703785.1:n.1148C=
ENST00000262464.9:c.4283C= MANE Select	ENSP00000262464.4:p.Thr1428=
ENST00000262464.8:c.4283C=	ENSP00000262464.4:p.Thr1428=
ENST00000507835.5:c.833C=	ENSP00000426839.1:p.Thr278=
ENST00000508053.5:c.4283C=	ENSP00000424571.1:p.Thr1428=
ENST00000508989.5:c.4184C=	ENSP00000425596.1:p.Thr1395=
ENST00000619499.4:c.4280C=	ENSP00000482132.1:p.Thr1427=
NM_001999.3:c.4283C=	NP_001990.2:p.Thr1428=
XM_017009228.2:c.4130C=	XP_016864717.1:p.Thr1377=
NM_001999.4:c.4283C= MANE Select	NP_001990.2:p.Thr1428=