Canonical Allele Identifier: CA2789960200
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129468307G>T , CM000672.2:g.129468307G>T GRCh38
NC_000010.10:g.131266571G>T , CM000672.1:g.131266571G>T GRCh37
NC_000010.9:g.131156561G>T NCBI36
NG_052673.1:g.6124G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.81+1011G>T ENSP00000302111.7:n.81+1011G>T
ENST00000651593.1:c.-13+1011G>T MANE Select ENSP00000498729.1:n.-13+1011G>T
ENST00000306010.7:c.81+1011G>T ENSP00000302111.7:n.81+1011G>T
ENST00000482547.1:n.35+1011G>T
ENST00000482653.1:n.68+1011G>T
NM_002412.3:c.81+1011G>T NP_002403.2:n.81+1011G>T
NM_002412.4:c.81+1011G>T NP_002403.2:n.81+1011G>T
XM_005252682.2:c.-13+866G>T XP_005252739.1:n.-13+866G>T
NM_002412.5:c.-13+1011G>T MANE Select NP_002403.3:n.-13+1011G>T