Canonical Allele Identifier: CA127008180

Gene: FBN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128334766T>C , CM000667.2:g.128334766T>C	GRCh38
NC_000005.9:g.127670458T>C , CM000667.1:g.127670458T>C	GRCh37
NC_000005.8:g.127698357T>C	NCBI36
NG_008750.1:g.208278A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001999.4:c.4052A>G MANE Select	NP_001990.2:p.His1351Arg
ENST00000262464.9:c.4052A>G MANE Select	ENSP00000262464.4:p.His1351Arg
NM_001999.3:c.4052A>G	NP_001990.2:p.His1351Arg
ENST00000262464.8:c.4052A>G	ENSP00000262464.4:p.His1351Arg
ENST00000507835.5:c.602A>G	ENSP00000426839.1:p.His201Arg
ENST00000508053.5:c.4052A>G	ENSP00000424571.1:p.His1351Arg
ENST00000508989.5:c.3953A>G	ENSP00000425596.1:p.His1318Arg
ENST00000619499.4:c.4049A>G	ENSP00000482132.1:p.His1350Arg
ENST00000703783.1:n.836A>G
ENST00000703785.1:n.917A>G
XM_017009228.2:c.3899A>G	XP_016864717.1:p.His1300Arg