Canonical Allele Identifier: CA1581268407
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128333000G= , CM000667.2:g.128333000G= GRCh38
NC_000005.9:g.127668692G= , CM000667.1:g.127668692G= GRCh37
NC_000005.8:g.127696591G= NCBI36
NG_008750.1:g.210044C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.918C=
ENST00000703785.1:n.999C=
ENST00000262464.9:c.4134C= MANE Select ENSP00000262464.4:p.Cys1378=
ENST00000262464.8:c.4134C= ENSP00000262464.4:p.Cys1378=
ENST00000507835.5:c.684C= ENSP00000426839.1:p.Cys228=
ENST00000508053.5:c.4134C= ENSP00000424571.1:p.Cys1378=
ENST00000508989.5:c.4035C= ENSP00000425596.1:p.Cys1345=
ENST00000619499.4:c.4131C= ENSP00000482132.1:p.Cys1377=
NM_001999.3:c.4134C= NP_001990.2:p.Cys1378=
XM_017009228.2:c.3981C= XP_016864717.1:p.Cys1327=
NM_001999.4:c.4134C= MANE Select NP_001990.2:p.Cys1378=