Canonical Allele Identifier: CA378713318
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766986G>C , CM000672.2:g.129766986G>C GRCh38
NC_000010.10:g.131565250G>C , CM000672.1:g.131565250G>C GRCh37
NC_000010.9:g.131455240G>C NCBI36
NG_052673.1:g.304803G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.706G>C ENSP00000302111.7:p.Gly236Arg
ENST00000651593.1:c.613G>C MANE Select ENSP00000498729.1:p.Gly205Arg
ENST00000306010.7:c.706G>C ENSP00000302111.7:p.Gly236Arg
NM_002412.3:c.706G>C NP_002403.2:p.Gly236Arg
NM_002412.4:c.706G>C NP_002403.2:p.Gly236Arg
XM_005252682.2:c.613G>C XP_005252739.1:p.Gly205Arg
XM_006717863.2:c.436G>C XP_006717926.1:p.Gly146Arg
XM_011539817.1:c.622G>C XP_011538119.1:p.Gly208Arg
NM_002412.5:c.613G>C MANE Select NP_002403.3:p.Gly205Arg
XM_017016275.1:c.436G>C XP_016871764.1:p.Gly146Arg