Canonical Allele Identifier: CA1581269566
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335394G= , CM000667.2:g.128335394G= GRCh38
NC_000005.9:g.127671086G= , CM000667.1:g.127671086G= GRCh37
NC_000005.8:g.127698985G= NCBI36
NG_008750.1:g.207650C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.631+61C=
ENST00000703785.1:n.712+61C=
ENST00000262464.9:c.3847+61C= MANE Select ENSP00000262464.4:n.3847+61C=
ENST00000262464.8:c.3847+61C= ENSP00000262464.4:n.3847+61C=
ENST00000507835.5:c.397+61C= ENSP00000426839.1:n.397+61C=
ENST00000508053.5:c.3847+61C= ENSP00000424571.1:n.3847+61C=
ENST00000508989.5:c.3748+61C= ENSP00000425596.1:n.3748+61C=
ENST00000619499.4:c.3844+61C= ENSP00000482132.1:n.3844+61C=
NM_001999.3:c.3847+61C= NP_001990.2:n.3847+61C=
XM_017009228.2:c.3694+61C= XP_016864717.1:n.3694+61C=
NM_001999.4:c.3847+61C= MANE Select NP_001990.2:n.3847+61C=