Canonical Allele Identifier: CA933838628
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1848948199
gnomAD v3: 10-129767116-G-A
gnomAD v4: 10-129767116-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767116G>A , CM000672.2:g.129767116G>A GRCh38
NC_000010.10:g.131565380G>A , CM000672.1:g.131565380G>A GRCh37
NC_000010.9:g.131455370G>A NCBI36
NG_052673.1:g.304933G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*119G>A ENSP00000302111.7:n.*119G>A
ENST00000651593.1:c.*119G>A MANE Select ENSP00000498729.1:n.*119G>A
ENST00000306010.7:c.*119G>A ENSP00000302111.7:n.*119G>A
NM_002412.3:c.*119G>A NP_002403.2:n.*119G>A
NM_002412.4:c.*119G>A NP_002403.2:n.*119G>A
XM_006717863.2:c.*119G>A XP_006717926.1:n.*119G>A
XM_011539817.1:c.*119G>A XP_011538119.1:n.*119G>A
NM_002412.5:c.*119G>A MANE Select NP_002403.3:n.*119G>A
XM_017016275.1:c.*119G>A XP_016871764.1:n.*119G>A
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