Canonical Allele Identifier: CA360757913
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335465T>A , CM000667.2:g.128335465T>A GRCh38
NC_000005.9:g.127671157T>A , CM000667.1:g.127671157T>A GRCh37
NC_000005.8:g.127699056T>A NCBI36
NG_008750.1:g.207579A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.621A>T
ENST00000703785.1:n.702A>T
ENST00000262464.9:c.3837A>T MANE Select ENSP00000262464.4:p.Arg1279Ser
ENST00000262464.8:c.3837A>T ENSP00000262464.4:p.Arg1279Ser
ENST00000507835.5:c.387A>T ENSP00000426839.1:p.Arg129Ser
ENST00000508053.5:c.3837A>T ENSP00000424571.1:p.Arg1279Ser
ENST00000508989.5:c.3738A>T ENSP00000425596.1:p.Arg1246Ser
ENST00000619499.4:c.3834A>T ENSP00000482132.1:p.Arg1278Ser
NM_001999.3:c.3837A>T NP_001990.2:p.Arg1279Ser
XM_017009228.2:c.3684A>T XP_016864717.1:p.Arg1228Ser
NM_001999.4:c.3837A>T MANE Select NP_001990.2:p.Arg1279Ser