Canonical Allele Identifier: CA2675116618
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128330573dup , CM000667.2:g.128330573dup GRCh38
NC_000005.9:g.127666265dup , CM000667.1:g.127666265dup GRCh37
NC_000005.8:g.127694164dup NCBI36
NG_008750.1:g.212472dup

Transcript Alleles

HGVS Amino-acid change
ENST00000703783.1:n.1129+1dup
ENST00000703785.1:n.1210+1dup
ENST00000262464.9:c.4345+1dup
ENST00000262464.8:c.4345+1dup
ENST00000507835.5:c.895+1dup
ENST00000508053.5:c.4345+1dup
ENST00000508989.5:c.4246+1dup
ENST00000619499.4:c.4342+1dup
NM_001999.3:c.4345+1dup
XM_017009228.2:c.4192+1dup
NM_001999.4:c.4345+1dup