Canonical Allele Identifier: CA360757926
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335471A>T , CM000667.2:g.128335471A>T GRCh38
NC_000005.9:g.127671163A>T , CM000667.1:g.127671163A>T GRCh37
NC_000005.8:g.127699062A>T NCBI36
NG_008750.1:g.207573T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.615T>A
ENST00000703785.1:n.696T>A
ENST00000262464.9:c.3831T>A MANE Select ENSP00000262464.4:p.Asp1277Glu
ENST00000262464.8:c.3831T>A ENSP00000262464.4:p.Asp1277Glu
ENST00000507835.5:c.381T>A ENSP00000426839.1:p.Asp127Glu
ENST00000508053.5:c.3831T>A ENSP00000424571.1:p.Asp1277Glu
ENST00000508989.5:c.3732T>A ENSP00000425596.1:p.Asp1244Glu
ENST00000619499.4:c.3828T>A ENSP00000482132.1:p.Asp1276Glu
NM_001999.3:c.3831T>A NP_001990.2:p.Asp1277Glu
XM_017009228.2:c.3678T>A XP_016864717.1:p.Asp1226Glu
NM_001999.4:c.3831T>A MANE Select NP_001990.2:p.Asp1277Glu