Canonical Allele Identifier: CA1581270732

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128338033C= , CM000667.2:g.128338033C=	GRCh38
NC_000005.9:g.127673725C= , CM000667.1:g.127673725C=	GRCh37
NC_000005.8:g.127701624C=	NCBI36
NG_008750.1:g.205011G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.346G=
ENST00000703785.1:n.427G=
ENST00000262464.9:c.3562G= MANE Select	ENSP00000262464.4:p.Gly1188=
ENST00000262464.8:c.3562G=	ENSP00000262464.4:p.Gly1188=
ENST00000507835.5:c.112G=	ENSP00000426839.1:p.Gly38=
ENST00000508053.5:c.3562G=	ENSP00000424571.1:p.Gly1188=
ENST00000508989.5:c.3463G=	ENSP00000425596.1:p.Gly1155=
ENST00000619499.4:c.3559G=	ENSP00000482132.1:p.Gly1187=
NM_001999.3:c.3562G=	NP_001990.2:p.Gly1188=
XM_017009228.2:c.3409G=	XP_016864717.1:p.Gly1137=
NM_001999.4:c.3562G= MANE Select	NP_001990.2:p.Gly1188=