Canonical Allele Identifier: CA650273020
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128527807A>T , CM000667.2:g.128527807A>T GRCh38
NC_000005.9:g.127863500A>T , CM000667.1:g.127863500A>T GRCh37
NC_000005.8:g.127891399A>T NCBI36
NG_008750.1:g.15236T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000508053.6:c.532+65T>A ENSP00000424571.2:n.532+65T>A
ENST00000703787.1:n.239+65T>A
ENST00000262464.9:c.532+65T>A MANE Select ENSP00000262464.4:n.532+65T>A
ENST00000262464.8:c.532+65T>A ENSP00000262464.4:n.532+65T>A
ENST00000502468.5:c.532+65T>A ENSP00000424753.1:n.532+65T>A
ENST00000508053.5:c.532+65T>A ENSP00000424571.1:n.532+65T>A
ENST00000508989.5:c.433+65T>A ENSP00000425596.1:n.433+65T>A
ENST00000514742.1:n.1152+65T>A
ENST00000619499.4:c.532+65T>A ENSP00000482132.1:n.532+65T>A
ENST00000620257.1:c.532+65T>A ENSP00000479157.1:n.532+65T>A
NM_001999.3:c.532+65T>A NP_001990.2:n.532+65T>A
XM_017009228.2:c.532+65T>A XP_016864717.1:n.532+65T>A
NM_001999.4:c.532+65T>A MANE Select NP_001990.2:n.532+65T>A