Canonical Allele Identifier: CA1581268548

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128333296C= , CM000667.2:g.128333296C=	GRCh38
NC_000005.9:g.127668988C= , CM000667.1:g.127668988C=	GRCh37
NC_000005.8:g.127696887C=	NCBI36
NG_008750.1:g.209748G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.884-262G=
ENST00000703785.1:n.965-262G=
ENST00000262464.9:c.4100-262G= MANE Select	ENSP00000262464.4:n.4100-262G=
ENST00000262464.8:c.4100-262G=	ENSP00000262464.4:n.4100-262G=
ENST00000507835.5:c.650-262G=	ENSP00000426839.1:n.650-262G=
ENST00000508053.5:c.4100-262G=	ENSP00000424571.1:n.4100-262G=
ENST00000508989.5:c.4001-262G=	ENSP00000425596.1:n.4001-262G=
ENST00000619499.4:c.4097-262G=	ENSP00000482132.1:n.4097-262G=
NM_001999.3:c.4100-262G=	NP_001990.2:n.4100-262G=
XM_017009228.2:c.3947-262G=	XP_016864717.1:n.3947-262G=
NM_001999.4:c.4100-262G= MANE Select	NP_001990.2:n.4100-262G=