Canonical Allele Identifier: CA471931541
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1334064777
gnomAD v2: 10-131265548-C-A
gnomAD v4: 10-129467284-C-A
MyVariant Identifiers: chr10:g.131265548C>A (hg19) chr10:g.129467284C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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