Canonical Allele Identifier: CA619544263
Community Standard Title: NM_002168.4(IDH2):c.*19G>A
Gene: IDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90084247C>T , CM000677.2:g.90084247C>T GRCh38
NC_000015.9:g.90627479C>T , CM000677.1:g.90627479C>T GRCh37
NC_000015.8:g.88428483C>T NCBI36
NG_023302.1:g.23230G>A , LRG_611:g.23230G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002168.4:c.*19G>A MANE Select NP_002159.2:n.*19G>A
ENST00000330062.8:c.*19G>A MANE Select ENSP00000331897.4:n.*19G>A
NM_001289910.1:c.*19G>A , LRG_611t1:c.*19G>A NP_001276839.1:n.*19G>A
NM_001290114.1:c.*19G>A NP_001277043.1:n.*19G>A
NM_001290114.2:c.*19G>A NP_001277043.1:n.*19G>A
NM_002168.3:c.*19G>A , LRG_611t2:c.*19G>A NP_002159.2:n.*19G>A
ENST00000330062.7:c.*19G>A ENSP00000331897.3:n.*19G>A
ENST00000540499.2:c.*19G>A ENSP00000446147.2:n.*19G>A
ENST00000559482.5:c.*19G>A ENSP00000453016.1:n.*19G>A
ENST00000560061.1:c.*1003G>A ENSP00000453254.1:n.*1003G>A