Canonical Allele Identifier: CA1581267330
Gene: FBN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128330563T= , CM000667.2:g.128330563T= GRCh38
NC_000005.9:g.127666255T= , CM000667.1:g.127666255T= GRCh37
NC_000005.8:g.127694154T= NCBI36
NG_008750.1:g.212481A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.1129+10A=
ENST00000703785.1:n.1210+10A=
ENST00000262464.9:c.4345+10A= MANE Select ENSP00000262464.4:n.4345+10A=
ENST00000262464.8:c.4345+10A= ENSP00000262464.4:n.4345+10A=
ENST00000507835.5:c.895+10A= ENSP00000426839.1:n.895+10A=
ENST00000508053.5:c.4345+10A= ENSP00000424571.1:n.4345+10A=
ENST00000508989.5:c.4246+10A= ENSP00000425596.1:n.4246+10A=
ENST00000619499.4:c.4342+10A= ENSP00000482132.1:n.4342+10A=
NM_001999.3:c.4345+10A= NP_001990.2:n.4345+10A=
XM_017009228.2:c.4192+10A= XP_016864717.1:n.4192+10A=
NM_001999.4:c.4345+10A= MANE Select NP_001990.2:n.4345+10A=