Canonical Allele Identifier: CA5747879
Gene: MGMT HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 376361
ClinVar RCV Id: RCV000431439
dbSNP Id: rs16906252

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467281C>T , CM000672.2:g.129467281C>T GRCh38
NC_000010.9:g.131155535C>T NCBI36
NC_000010.10:g.131265545C>T , CM000672.1:g.131265545C>T GRCh37
NG_052673.1:g.5098C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.7:c.66C>T ENSP00000302111.7:p.Arg22=
ENST00000482547.1:n.20C>T
ENST00000482653.1:n.53C>T
NM_002412.3:c.66C>T VV
NM_002412.4:c.66C>T VV NP_002403.2:p.Arg22=
NM_002412.5:c.-28C>T VV NP_002403.3:p.=