Canonical Allele Identifier: CA2675114531
Gene: FBN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128305106del , CM000667.2:g.128305106del GRCh38
NC_000005.9:g.127640798del , CM000667.1:g.127640798del GRCh37
NC_000005.8:g.127668697del NCBI36
NG_008750.1:g.237939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.2459-23del
ENST00000703785.1:n.2378-23del
ENST00000262464.9:c.5675-23del MANE Select ENSP00000262464.4:n.5675-23del
ENST00000262464.8:c.5675-23del ENSP00000262464.4:n.5675-23del
ENST00000508053.5:c.5675-23del ENSP00000424571.1:n.5675-23del
ENST00000619499.4:c.5672-23del ENSP00000482132.1:n.5672-23del
NM_001999.3:c.5675-23del NP_001990.2:n.5675-23del
XM_017009228.2:c.5522-23del XP_016864717.1:n.5522-23del
NM_001999.4:c.5675-23del MANE Select NP_001990.2:n.5675-23del