Canonical Allele Identifier: CA1581270699

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128337961G= , CM000667.2:g.128337961G=	GRCh38
NC_000005.9:g.127673653G= , CM000667.1:g.127673653G=	GRCh37
NC_000005.8:g.127701552G=	NCBI36
NG_008750.1:g.205083C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703783.1:n.382+36C=
ENST00000703785.1:n.463+36C=
ENST00000262464.9:c.3598+36C= MANE Select	ENSP00000262464.4:n.3598+36C=
ENST00000262464.8:c.3598+36C=	ENSP00000262464.4:n.3598+36C=
ENST00000507835.5:c.148+36C=	ENSP00000426839.1:n.148+36C=
ENST00000508053.5:c.3598+36C=	ENSP00000424571.1:n.3598+36C=
ENST00000508989.5:c.3499+36C=	ENSP00000425596.1:n.3499+36C=
ENST00000619499.4:c.3595+36C=	ENSP00000482132.1:n.3595+36C=
NM_001999.3:c.3598+36C=	NP_001990.2:n.3598+36C=
XM_017009228.2:c.3445+36C=	XP_016864717.1:n.3445+36C=
NM_001999.4:c.3598+36C= MANE Select	NP_001990.2:n.3598+36C=