Canonical Allele Identifier: CA378713281

Gene: MGMT

Linked Data

• dbSNP Id: rs766247777
• MyVariant Identifiers: chr10:g.131565229A>G (hg19) ; chr10:g.129766965A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766965A>G , CM000672.2:g.129766965A>G	GRCh38
NC_000010.10:g.131565229A>G , CM000672.1:g.131565229A>G	GRCh37
NC_000010.9:g.131455219A>G	NCBI36
NG_052673.1:g.304782A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.685A>G	ENSP00000302111.7:p.Thr229Ala
ENST00000651593.1:c.592A>G MANE Select	ENSP00000498729.1:p.Thr198Ala
ENST00000306010.7:c.685A>G	ENSP00000302111.7:p.Thr229Ala
NM_002412.3:c.685A>G	NP_002403.2:p.Thr229Ala
NM_002412.4:c.685A>G	NP_002403.2:p.Thr229Ala
XM_005252682.2:c.592A>G	XP_005252739.1:p.Thr198Ala
XM_006717863.2:c.415A>G	XP_006717926.1:p.Thr139Ala
XM_011539817.1:c.601A>G	XP_011538119.1:p.Thr201Ala
NM_002412.5:c.592A>G MANE Select	NP_002403.3:p.Thr198Ala
XM_017016275.1:c.415A>G	XP_016871764.1:p.Thr139Ala