Canonical Allele Identifier: CA1581269635
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335563T= , CM000667.2:g.128335563T= GRCh38
NC_000005.9:g.127671255T= , CM000667.1:g.127671255T= GRCh37
NC_000005.8:g.127699154T= NCBI36
NG_008750.1:g.207481A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.523A=
ENST00000703785.1:n.604A=
ENST00000262464.9:c.3739A= MANE Select ENSP00000262464.4:p.Met1247=
ENST00000262464.8:c.3739A= ENSP00000262464.4:p.Met1247=
ENST00000507835.5:c.289A= ENSP00000426839.1:p.Met97=
ENST00000508053.5:c.3739A= ENSP00000424571.1:p.Met1247=
ENST00000508989.5:c.3640A= ENSP00000425596.1:p.Met1214=
ENST00000619499.4:c.3736A= ENSP00000482132.1:p.Met1246=
NM_001999.3:c.3739A= NP_001990.2:p.Met1247=
XM_017009228.2:c.3586A= XP_016864717.1:p.Met1196=
NM_001999.4:c.3739A= MANE Select NP_001990.2:p.Met1247=