Canonical Allele Identifier: CA393802508
Gene: IDH2 HGNC NCBI

Linked Data

dbSNP Id: rs2151549903

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90088736T>A , CM000677.2:g.90088736T>A GRCh38
NC_000015.9:g.90631968T>A , CM000677.1:g.90631968T>A GRCh37
NC_000015.8:g.88432972T>A NCBI36
NG_023302.1:g.18741A>T , LRG_611:g.18741A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330062.8:c.385A>T MANE Select ENSP00000331897.4:p.Lys129Ter
ENST00000330062.7:c.385A>T ENSP00000331897.3:p.Lys129Ter
ENST00000540499.2:c.229A>T ENSP00000446147.2:p.Lys77Ter
ENST00000559482.5:c.208-234A>T ENSP00000453016.1:n.208-234A>T
ENST00000560061.1:c.*10A>T ENSP00000453254.1:n.*10A>T
NM_001289910.1:c.229A>T , LRG_611t1:c.229A>T NP_001276839.1:p.Lys77Ter
NM_001290114.1:c.-6A>T NP_001277043.1:n.-6A>T
NM_002168.3:c.385A>T , LRG_611t2:c.385A>T NP_002159.2:p.Lys129Ter
NM_001290114.2:c.-6A>T NP_001277043.1:n.-6A>T
NM_002168.4:c.385A>T MANE Select NP_002159.2:p.Lys129Ter