Canonical Allele Identifier: CA1581268408
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333001C= , CM000667.2:g.128333001C= GRCh38
NC_000005.9:g.127668693C= , CM000667.1:g.127668693C= GRCh37
NC_000005.8:g.127696592C= NCBI36
NG_008750.1:g.210043G=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.917G=
ENST00000703785.1:n.998G=
ENST00000262464.9:c.4133G= MANE Select ENSP00000262464.4:p.Cys1378=
ENST00000262464.8:c.4133G= ENSP00000262464.4:p.Cys1378=
ENST00000507835.5:c.683G= ENSP00000426839.1:p.Cys228=
ENST00000508053.5:c.4133G= ENSP00000424571.1:p.Cys1378=
ENST00000508989.5:c.4034G= ENSP00000425596.1:p.Cys1345=
ENST00000619499.4:c.4130G= ENSP00000482132.1:p.Cys1377=
NM_001999.3:c.4133G= NP_001990.2:p.Cys1378=
XM_017009228.2:c.3980G= XP_016864717.1:p.Cys1327=
NM_001999.4:c.4133G= MANE Select NP_001990.2:p.Cys1378=