Canonical Allele Identifier: CA1581269591

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335449C= , CM000667.2:g.128335449C=	GRCh38
NC_000005.9:g.127671141C= , CM000667.1:g.127671141C=	GRCh37
NC_000005.8:g.127699040C=	NCBI36
NG_008750.1:g.207595G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703783.1:n.631+6G=
ENST00000703785.1:n.712+6G=
ENST00000262464.9:c.3847+6G= MANE Select	ENSP00000262464.4:n.3847+6G=
ENST00000262464.8:c.3847+6G=	ENSP00000262464.4:n.3847+6G=
ENST00000507835.5:c.397+6G=	ENSP00000426839.1:n.397+6G=
ENST00000508053.5:c.3847+6G=	ENSP00000424571.1:n.3847+6G=
ENST00000508989.5:c.3748+6G=	ENSP00000425596.1:n.3748+6G=
ENST00000619499.4:c.3844+6G=	ENSP00000482132.1:n.3844+6G=
NM_001999.3:c.3847+6G=	NP_001990.2:n.3847+6G=
XM_017009228.2:c.3694+6G=	XP_016864717.1:n.3694+6G=
NM_001999.4:c.3847+6G= MANE Select	NP_001990.2:n.3847+6G=