Canonical Allele Identifier: CA1581267301
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128330485C= , CM000667.2:g.128330485C= GRCh38
NC_000005.9:g.127666177C= , CM000667.1:g.127666177C= GRCh37
NC_000005.8:g.127694076C= NCBI36
NG_008750.1:g.212559G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.1129+88G=
ENST00000703785.1:n.1210+88G=
ENST00000262464.9:c.4345+88G= MANE Select ENSP00000262464.4:n.4345+88G=
ENST00000262464.8:c.4345+88G= ENSP00000262464.4:n.4345+88G=
ENST00000507835.5:c.895+88G= ENSP00000426839.1:n.895+88G=
ENST00000508053.5:c.4345+88G= ENSP00000424571.1:n.4345+88G=
ENST00000508989.5:c.4246+88G= ENSP00000425596.1:n.4246+88G=
ENST00000619499.4:c.4342+88G= ENSP00000482132.1:n.4342+88G=
NM_001999.3:c.4345+88G= NP_001990.2:n.4345+88G=
XM_017009228.2:c.4192+88G= XP_016864717.1:n.4192+88G=
NM_001999.4:c.4345+88G= MANE Select NP_001990.2:n.4345+88G=