Canonical Allele Identifier: CA1581267341

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128330593C= , CM000667.2:g.128330593C=	GRCh38
NC_000005.9:g.127666285C= , CM000667.1:g.127666285C=	GRCh37
NC_000005.8:g.127694184C=	NCBI36
NG_008750.1:g.212451G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.1109G=
ENST00000703785.1:n.1190G=
ENST00000262464.9:c.4325G= MANE Select	ENSP00000262464.4:p.Gly1442=
ENST00000262464.8:c.4325G=	ENSP00000262464.4:p.Gly1442=
ENST00000507835.5:c.875G=	ENSP00000426839.1:p.Gly292=
ENST00000508053.5:c.4325G=	ENSP00000424571.1:p.Gly1442=
ENST00000508989.5:c.4226G=	ENSP00000425596.1:p.Gly1409=
ENST00000619499.4:c.4322G=	ENSP00000482132.1:p.Gly1441=
NM_001999.3:c.4325G=	NP_001990.2:p.Gly1442=
XM_017009228.2:c.4172G=	XP_016864717.1:p.Gly1391=
NM_001999.4:c.4325G= MANE Select	NP_001990.2:p.Gly1442=