Canonical Allele Identifier: CA360750621
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395181T>A , CM000667.2:g.128395181T>A GRCh38
NC_000005.9:g.127730874T>A , CM000667.1:g.127730874T>A GRCh37
NC_000005.8:g.127758773T>A NCBI36
NG_008750.1:g.147862A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703787.1:n.879A>T
ENST00000262464.9:c.1172A>T MANE Select ENSP00000262464.4:p.Glu391Val
ENST00000262464.8:c.1172A>T ENSP00000262464.4:p.Glu391Val
ENST00000508053.5:c.1172A>T ENSP00000424571.1:p.Glu391Val
ENST00000508989.5:c.1073A>T ENSP00000425596.1:p.Glu358Val
ENST00000619499.4:c.1169A>T ENSP00000482132.1:p.Glu390Val
NM_001999.3:c.1172A>T NP_001990.2:p.Glu391Val
XM_017009228.2:c.1079-1813A>T XP_016864717.1:n.1079-1813A>T
NM_001999.4:c.1172A>T MANE Select NP_001990.2:p.Glu391Val