Canonical Allele Identifier: CA1944760002
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467284C= , CM000672.2:g.129467284C= GRCh38
NC_000010.10:g.131265548C= , CM000672.1:g.131265548C= GRCh37
NC_000010.9:g.131155538C= NCBI36
NG_052673.1:g.5101C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.69C= ENSP00000302111.7:p.Thr23=
ENST00000651593.1:c.-25C= MANE Select ENSP00000498729.1:n.-25C=
ENST00000306010.7:c.69C= ENSP00000302111.7:p.Thr23=
ENST00000482547.1:n.23C=
ENST00000482653.1:n.56C=
NM_002412.3:c.69C= NP_002403.2:p.Thr23=
NM_002412.4:c.69C= NP_002403.2:p.Thr23=
NM_002412.5:c.-25C= MANE Select NP_002403.3:n.-25C=