Canonical Allele Identifier: CA2194954296
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088320T= , CM000677.2:g.90088320T= GRCh38
NC_000015.9:g.90631552T= , CM000677.1:g.90631552T= GRCh37
NC_000015.8:g.88432556T= NCBI36
NG_023302.1:g.19157A= , LRG_611:g.19157A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.678+39A= MANE Select ENSP00000331897.4:n.678+39A=
ENST00000330062.7:c.678+39A= ENSP00000331897.3:n.678+39A=
ENST00000540499.2:c.522+39A= ENSP00000446147.2:n.522+39A=
ENST00000559482.5:c.351+39A= ENSP00000453016.1:n.351+39A=
ENST00000560061.1:c.*303+39A= ENSP00000453254.1:n.*303+39A=
NM_001289910.1:c.522+39A= , LRG_611t1:c.522+39A= NP_001276839.1:n.522+39A=
NM_001290114.1:c.288+39A= NP_001277043.1:n.288+39A=
NM_002168.3:c.678+39A= , LRG_611t2:c.678+39A= NP_002159.2:n.678+39A=
NM_001290114.2:c.288+39A= NP_001277043.1:n.288+39A=
NM_002168.4:c.678+39A= MANE Select NP_002159.2:n.678+39A=