Canonical Allele Identifier: CA1581295529
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128395202G= , CM000667.2:g.128395202G= GRCh38
NC_000005.9:g.127730895G= , CM000667.1:g.127730895G= GRCh37
NC_000005.8:g.127758794G= NCBI36
NG_008750.1:g.147841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703787.1:n.858C=
ENST00000262464.9:c.1151C= MANE Select ENSP00000262464.4:p.Thr384=
ENST00000262464.8:c.1151C= ENSP00000262464.4:p.Thr384=
ENST00000508053.5:c.1151C= ENSP00000424571.1:p.Thr384=
ENST00000508989.5:c.1052C= ENSP00000425596.1:p.Thr351=
ENST00000619499.4:c.1148C= ENSP00000482132.1:p.Thr383=
NM_001999.3:c.1151C= NP_001990.2:p.Thr384=
XM_017009228.2:c.1079-1834C= XP_016864717.1:n.1079-1834C=
NM_001999.4:c.1151C= MANE Select NP_001990.2:p.Thr384=