Canonical Allele Identifier: CA378909655
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129467289-G-A
MyVariant Identifiers: chr10:g.131265553G>A (hg19) chr10:g.129467289G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467289G>A , CM000672.2:g.129467289G>A GRCh38
NC_000010.10:g.131265553G>A , CM000672.1:g.131265553G>A GRCh37
NC_000010.9:g.131155543G>A NCBI36
NG_052673.1:g.5106G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.74G>A ENSP00000302111.7:p.Cys25Tyr
ENST00000651593.1:c.-20G>A MANE Select ENSP00000498729.1:n.-20G>A
ENST00000306010.7:c.74G>A ENSP00000302111.7:p.Cys25Tyr
ENST00000482547.1:n.28G>A
ENST00000482653.1:n.61G>A
NM_002412.3:c.74G>A NP_002403.2:p.Cys25Tyr
NM_002412.4:c.74G>A NP_002403.2:p.Cys25Tyr
NM_002412.5:c.-20G>A MANE Select NP_002403.3:n.-20G>A
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