Canonical Allele Identifier: CA933839881
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1847166342
gnomAD v3: 10-129627688-G-A
gnomAD v4: 10-129627688-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627688G>A , CM000672.2:g.129627688G>A GRCh38
NC_000010.10:g.131425952G>A , CM000672.1:g.131425952G>A GRCh37
NC_000010.9:g.131315942G>A NCBI36
NG_052673.1:g.165505G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.219-80207G>A ENSP00000302111.7:n.219-80207G>A
ENST00000651593.1:c.126-80207G>A MANE Select ENSP00000498729.1:n.126-80207G>A
ENST00000306010.7:c.219-80207G>A ENSP00000302111.7:n.219-80207G>A
NM_002412.3:c.219-80207G>A NP_002403.2:n.219-80207G>A
NM_002412.4:c.219-80207G>A NP_002403.2:n.219-80207G>A
XM_005252682.2:c.126-80207G>A XP_005252739.1:n.126-80207G>A
XM_006717863.2:c.-125-19074G>A XP_006717926.1:n.-125-19074G>A
XM_011539817.1:c.-3-19074G>A XP_011538119.1:n.-3-19074G>A
NM_002412.5:c.126-80207G>A MANE Select NP_002403.3:n.126-80207G>A
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