Canonical Allele Identifier: CA3131046677
Community Standard Title: NM_001999.4(FBN2):c.3832G= (p.Gly1278=)
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335470C= , CM000667.2:g.128335470C= GRCh38
NC_000005.9:g.127671162C= , CM000667.1:g.127671162C= GRCh37
NC_000005.8:g.127699061C= NCBI36
NG_008750.1:g.207574G=

Transcript Alleles

HGVS Amino-acid Change
NM_001999.4:c.3832G= MANE Select NP_001990.2:p.Gly1278=
ENST00000262464.9:c.3832G= MANE Select ENSP00000262464.4:p.Gly1278=
NM_001999.3:c.3832G= NP_001990.2:p.Gly1278=
ENST00000262464.8:c.3832G= ENSP00000262464.4:p.Gly1278=
ENST00000507835.5:c.382G= ENSP00000426839.1:p.Gly128=
ENST00000508053.5:c.3832G= ENSP00000424571.1:p.Gly1278=
ENST00000508989.5:c.3733G= ENSP00000425596.1:p.Gly1245=
ENST00000619499.4:c.3829G= ENSP00000482132.1:p.Gly1277=
ENST00000703783.1:n.616G=
ENST00000703785.1:n.697G=
XM_017009228.2:c.3679G= XP_016864717.1:p.Gly1227=