Canonical Allele Identifier: CA393802363

Gene: IDH2

Linked Data

• dbSNP Id: rs2151549691
• MyVariant Identifiers: chr15:g.90631898A>C (hg19) ; chr15:g.90088666A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90088666A>C , CM000677.2:g.90088666A>C	GRCh38
NC_000015.9:g.90631898A>C , CM000677.1:g.90631898A>C	GRCh37
NC_000015.8:g.88432902A>C	NCBI36
NG_023302.1:g.18811T>G , LRG_611:g.18811T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330062.8:c.455T>G MANE Select	ENSP00000331897.4:p.Ile152Ser
ENST00000330062.7:c.455T>G	ENSP00000331897.3:p.Ile152Ser
ENST00000540499.2:c.299T>G	ENSP00000446147.2:p.Ile100Ser
ENST00000559482.5:c.208-164T>G	ENSP00000453016.1:n.208-164T>G
ENST00000560061.1:c.*80T>G	ENSP00000453254.1:n.*80T>G
NM_001289910.1:c.299T>G , LRG_611t1:c.299T>G	NP_001276839.1:p.Ile100Ser
NM_001290114.1:c.65T>G	NP_001277043.1:p.Ile22Ser
NM_002168.3:c.455T>G , LRG_611t2:c.455T>G	NP_002159.2:p.Ile152Ser
NM_001290114.2:c.65T>G	NP_001277043.1:p.Ile22Ser
NM_002168.4:c.455T>G MANE Select	NP_002159.2:p.Ile152Ser