Canonical Allele Identifier: CA1581269637
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335572C= , CM000667.2:g.128335572C= GRCh38
NC_000005.9:g.127671264C= , CM000667.1:g.127671264C= GRCh37
NC_000005.8:g.127699163C= NCBI36
NG_008750.1:g.207472G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.514G=
ENST00000703785.1:n.595G=
ENST00000262464.9:c.3730G= MANE Select ENSP00000262464.4:p.Asp1244=
ENST00000262464.8:c.3730G= ENSP00000262464.4:p.Asp1244=
ENST00000507835.5:c.280G= ENSP00000426839.1:p.Asp94=
ENST00000508053.5:c.3730G= ENSP00000424571.1:p.Asp1244=
ENST00000508989.5:c.3631G= ENSP00000425596.1:p.Asp1211=
ENST00000619499.4:c.3727G= ENSP00000482132.1:p.Asp1243=
NM_001999.3:c.3730G= NP_001990.2:p.Asp1244=
XM_017009228.2:c.3577G= XP_016864717.1:p.Asp1193=
NM_001999.4:c.3730G= MANE Select NP_001990.2:p.Asp1244=