Canonical Allele Identifier: CA360758659
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128527956T>G , CM000667.2:g.128527956T>G GRCh38
NC_000005.9:g.127863649T>G , CM000667.1:g.127863649T>G GRCh37
NC_000005.8:g.127891548T>G NCBI36
NG_008750.1:g.15087A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000508053.6:c.448A>C ENSP00000424571.2:p.Ser150Arg
ENST00000703787.1:n.155A>C
ENST00000262464.9:c.448A>C MANE Select ENSP00000262464.4:p.Ser150Arg
ENST00000262464.8:c.448A>C ENSP00000262464.4:p.Ser150Arg
ENST00000502468.5:c.448A>C ENSP00000424753.1:p.Ser150Arg
ENST00000508053.5:c.448A>C ENSP00000424571.1:p.Ser150Arg
ENST00000508989.5:c.349A>C ENSP00000425596.1:p.Ser117Arg
ENST00000514742.1:n.1068A>C
ENST00000619499.4:c.448A>C ENSP00000482132.1:p.Ser150Arg
ENST00000620257.1:c.448A>C ENSP00000479157.1:p.Ser150Arg
NM_001999.3:c.448A>C NP_001990.2:p.Ser150Arg
XM_017009228.2:c.448A>C XP_016864717.1:p.Ser150Arg
NM_001999.4:c.448A>C MANE Select NP_001990.2:p.Ser150Arg