Canonical Allele Identifier: CA378909634
Gene: MGMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467282A>T , CM000672.2:g.129467282A>T GRCh38
NC_000010.10:g.131265546A>T , CM000672.1:g.131265546A>T GRCh37
NC_000010.9:g.131155536A>T NCBI36
NG_052673.1:g.5099A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.67A>T ENSP00000302111.7:p.Thr23Ser
ENST00000651593.1:c.-27A>T MANE Select ENSP00000498729.1:n.-27A>T
ENST00000306010.7:c.67A>T ENSP00000302111.7:p.Thr23Ser
ENST00000482547.1:n.21A>T
ENST00000482653.1:n.54A>T
NM_002412.3:c.67A>T NP_002403.2:p.Thr23Ser
NM_002412.4:c.67A>T NP_002403.2:p.Thr23Ser
NM_002412.5:c.-27A>T MANE Select NP_002403.3:n.-27A>T