Canonical Allele Identifier: CA360757296

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128335176A>G , CM000667.2:g.128335176A>G	GRCh38
NC_000005.9:g.127670868A>G , CM000667.1:g.127670868A>G	GRCh37
NC_000005.8:g.127698767A>G	NCBI36
NG_008750.1:g.207868T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001999.4:c.3967T>C MANE Select	NP_001990.2:p.Cys1323Arg
ENST00000262464.9:c.3967T>C MANE Select	ENSP00000262464.4:p.Cys1323Arg
NM_001999.3:c.3967T>C	NP_001990.2:p.Cys1323Arg
ENST00000262464.8:c.3967T>C	ENSP00000262464.4:p.Cys1323Arg
ENST00000507835.5:c.517T>C	ENSP00000426839.1:p.Cys173Arg
ENST00000508053.5:c.3967T>C	ENSP00000424571.1:p.Cys1323Arg
ENST00000508989.5:c.3868T>C	ENSP00000425596.1:p.Cys1290Arg
ENST00000619499.4:c.3964T>C	ENSP00000482132.1:p.Cys1322Arg
ENST00000703783.1:n.751T>C
ENST00000703785.1:n.832T>C
XM_017009228.2:c.3814T>C	XP_016864717.1:p.Cys1272Arg