Canonical Allele Identifier: CA393802541

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549947
• MyVariant Identifiers: chr15:g.90631981T>G (hg19) ; chr15:g.90088749T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088749T>G , CM000677.2:g.90088749T>G	GRCh38
NC_000015.9:g.90631981T>G , CM000677.1:g.90631981T>G	GRCh37
NC_000015.8:g.88432985T>G	NCBI36
NG_023302.1:g.18728A>C , LRG_611:g.18728A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.374-2A>C MANE Select	ENSP00000331897.4:n.374-2A>C
ENST00000330062.7:c.374-2A>C	ENSP00000331897.3:n.374-2A>C
ENST00000540499.2:c.218-2A>C	ENSP00000446147.2:n.218-2A>C
ENST00000559482.5:c.208-247A>C	ENSP00000453016.1:n.208-247A>C
ENST00000560061.1:c.116-2A>C	ENSP00000453254.1:n.116-2A>C
NM_001289910.1:c.218-2A>C , LRG_611t1:c.218-2A>C	NP_001276839.1:n.218-2A>C
NM_001290114.1:c.-17-2A>C	NP_001277043.1:n.-17-2A>C
NM_002168.3:c.374-2A>C , LRG_611t2:c.374-2A>C	NP_002159.2:n.374-2A>C
NM_001290114.2:c.-17-2A>C	NP_001277043.1:n.-17-2A>C
NM_002168.4:c.374-2A>C MANE Select	NP_002159.2:n.374-2A>C