Canonical Allele Identifier: CA5748153
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs752726386

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766911G>A , CM000672.2:g.129766911G>A GRCh38
NC_000010.10:g.131565175G>A , CM000672.1:g.131565175G>A GRCh37
NC_000010.9:g.131455165G>A NCBI36
NG_052673.1:g.304728G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.631G>A ENSP00000302111.7:p.Gly211Ser
ENST00000651593.1:c.538G>A MANE Select ENSP00000498729.1:p.Gly180Ser
ENST00000306010.7:c.631G>A ENSP00000302111.7:p.Gly211Ser
NM_002412.3:c.631G>A NP_002403.2:p.Gly211Ser
NM_002412.4:c.631G>A NP_002403.2:p.Gly211Ser
XM_005252682.2:c.538G>A XP_005252739.1:p.Gly180Ser
XM_006717863.2:c.361G>A XP_006717926.1:p.Gly121Ser
XM_011539817.1:c.547G>A XP_011538119.1:p.Gly183Ser
NM_002412.5:c.538G>A MANE Select NP_002403.3:p.Gly180Ser
XM_017016275.1:c.361G>A XP_016871764.1:p.Gly121Ser