Canonical Allele Identifier: CA378713227
Gene: MGMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.131565202G>A (hg19) chr10:g.129766938G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766938G>A , CM000672.2:g.129766938G>A GRCh38
NC_000010.10:g.131565202G>A , CM000672.1:g.131565202G>A GRCh37
NC_000010.9:g.131455192G>A NCBI36
NG_052673.1:g.304755G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.658G>A ENSP00000302111.7:p.Gly220Arg
ENST00000651593.1:c.565G>A MANE Select ENSP00000498729.1:p.Gly189Arg
ENST00000306010.7:c.658G>A ENSP00000302111.7:p.Gly220Arg
NM_002412.3:c.658G>A NP_002403.2:p.Gly220Arg
NM_002412.4:c.658G>A NP_002403.2:p.Gly220Arg
XM_005252682.2:c.565G>A XP_005252739.1:p.Gly189Arg
XM_006717863.2:c.388G>A XP_006717926.1:p.Gly130Arg
XM_011539817.1:c.574G>A XP_011538119.1:p.Gly192Arg
NM_002412.5:c.565G>A MANE Select NP_002403.3:p.Gly189Arg
XM_017016275.1:c.388G>A XP_016871764.1:p.Gly130Arg
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