Canonical Allele Identifier: CA2194954328
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088382T= , CM000677.2:g.90088382T= GRCh38
NC_000015.9:g.90631614T= , CM000677.1:g.90631614T= GRCh37
NC_000015.8:g.88432618T= NCBI36
NG_023302.1:g.19095A= , LRG_611:g.19095A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.655A= MANE Select ENSP00000331897.4:p.Met219=
ENST00000330062.7:c.655A= ENSP00000331897.3:p.Met219=
ENST00000540499.2:c.499A= ENSP00000446147.2:p.Met167=
ENST00000559482.5:c.328A= ENSP00000453016.1:p.Met110=
ENST00000560061.1:c.*280A= ENSP00000453254.1:n.*280A=
NM_001289910.1:c.499A= , LRG_611t1:c.499A= NP_001276839.1:p.Met167=
NM_001290114.1:c.265A= NP_001277043.1:p.Met89=
NM_002168.3:c.655A= , LRG_611t2:c.655A= NP_002159.2:p.Met219=
NM_001290114.2:c.265A= NP_001277043.1:p.Met89=
NM_002168.4:c.655A= MANE Select NP_002159.2:p.Met219=