Canonical Allele Identifier: CA2194954477
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088682C= , CM000677.2:g.90088682C= GRCh38
NC_000015.9:g.90631914C= , CM000677.1:g.90631914C= GRCh37
NC_000015.8:g.88432918C= NCBI36
NG_023302.1:g.18795G= , LRG_611:g.18795G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.439G= MANE Select ENSP00000331897.4:p.Val147=
ENST00000330062.7:c.439G= ENSP00000331897.3:p.Val147=
ENST00000540499.2:c.283G= ENSP00000446147.2:p.Val95=
ENST00000559482.5:c.208-180G= ENSP00000453016.1:n.208-180G=
ENST00000560061.1:c.*64G= ENSP00000453254.1:n.*64G=
NM_001289910.1:c.283G= , LRG_611t1:c.283G= NP_001276839.1:p.Val95=
NM_001290114.1:c.49G= NP_001277043.1:p.Val17=
NM_002168.3:c.439G= , LRG_611t2:c.439G= NP_002159.2:p.Val147=
NM_001290114.2:c.49G= NP_001277043.1:p.Val17=
NM_002168.4:c.439G= MANE Select NP_002159.2:p.Val147=