Canonical Allele Identifier: CA1581269511
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335272G= , CM000667.2:g.128335272G= GRCh38
NC_000005.9:g.127670964G= , CM000667.1:g.127670964G= GRCh37
NC_000005.8:g.127698863G= NCBI36
NG_008750.1:g.207772C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.655C=
ENST00000703785.1:n.736C=
ENST00000262464.9:c.3871C= MANE Select ENSP00000262464.4:p.Pro1291=
ENST00000262464.8:c.3871C= ENSP00000262464.4:p.Pro1291=
ENST00000507835.5:c.421C= ENSP00000426839.1:p.Pro141=
ENST00000508053.5:c.3871C= ENSP00000424571.1:p.Pro1291=
ENST00000508989.5:c.3772C= ENSP00000425596.1:p.Pro1258=
ENST00000619499.4:c.3868C= ENSP00000482132.1:p.Pro1290=
NM_001999.3:c.3871C= NP_001990.2:p.Pro1291=
XM_017009228.2:c.3718C= XP_016864717.1:p.Pro1240=
NM_001999.4:c.3871C= MANE Select NP_001990.2:p.Pro1291=