Canonical Allele Identifier: CA3396100
Gene: FBN2 HGNC NCBI

Linked Data

dbSNP Id: rs147157552

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128527886G>C , CM000667.2:g.128527886G>C GRCh38
NC_000005.9:g.127863579G>C , CM000667.1:g.127863579G>C GRCh37
NC_000005.8:g.127891478G>C NCBI36
NG_008750.1:g.15157C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000508053.6:c.518C>G ENSP00000424571.2:p.Thr173Ser
ENST00000703787.1:n.225C>G
ENST00000262464.9:c.518C>G MANE Select ENSP00000262464.4:p.Thr173Ser
ENST00000262464.8:c.518C>G ENSP00000262464.4:p.Thr173Ser
ENST00000502468.5:c.518C>G ENSP00000424753.1:p.Thr173Ser
ENST00000508053.5:c.518C>G ENSP00000424571.1:p.Thr173Ser
ENST00000508989.5:c.419C>G ENSP00000425596.1:p.Thr140Ser
ENST00000514742.1:n.1138C>G
ENST00000619499.4:c.518C>G ENSP00000482132.1:p.Thr173Ser
ENST00000620257.1:c.518C>G ENSP00000479157.1:p.Thr173Ser
NM_001999.3:c.518C>G NP_001990.2:p.Thr173Ser
XM_017009228.2:c.518C>G XP_016864717.1:p.Thr173Ser
NM_001999.4:c.518C>G MANE Select NP_001990.2:p.Thr173Ser