Canonical Allele Identifier: CA393802235

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549550
• gnomAD v4: 15-90088604-G-A
• MyVariant Identifiers: chr15:g.90631836G>A (hg19) ; chr15:g.90088604G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088604G>A , CM000677.2:g.90088604G>A	GRCh38
NC_000015.9:g.90631836G>A , CM000677.1:g.90631836G>A	GRCh37
NC_000015.8:g.88432840G>A	NCBI36
NG_023302.1:g.18873C>T , LRG_611:g.18873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.517C>T MANE Select	ENSP00000331897.4:p.His173Tyr
ENST00000330062.7:c.517C>T	ENSP00000331897.3:p.His173Tyr
ENST00000540499.2:c.361C>T	ENSP00000446147.2:p.His121Tyr
ENST00000559482.5:c.208-102C>T	ENSP00000453016.1:n.208-102C>T
ENST00000560061.1:c.*142C>T	ENSP00000453254.1:n.*142C>T
NM_001289910.1:c.361C>T , LRG_611t1:c.361C>T	NP_001276839.1:p.His121Tyr
NM_001290114.1:c.127C>T	NP_001277043.1:p.His43Tyr
NM_002168.3:c.517C>T , LRG_611t2:c.517C>T	NP_002159.2:p.His173Tyr
NM_001290114.2:c.127C>T	NP_001277043.1:p.His43Tyr
NM_002168.4:c.517C>T MANE Select	NP_002159.2:p.His173Tyr