Canonical Allele Identifier: CA2611438421
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129767154-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767154A>G , CM000672.2:g.129767154A>G GRCh38
NC_000010.10:g.131565418A>G , CM000672.1:g.131565418A>G GRCh37
NC_000010.9:g.131455408A>G NCBI36
NG_052673.1:g.304971A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*157A>G ENSP00000302111.7:n.*157A>G
ENST00000651593.1:c.*157A>G MANE Select ENSP00000498729.1:n.*157A>G
ENST00000306010.7:c.*157A>G ENSP00000302111.7:n.*157A>G
NM_002412.3:c.*157A>G NP_002403.2:n.*157A>G
NM_002412.4:c.*157A>G NP_002403.2:n.*157A>G
XM_006717863.2:c.*157A>G XP_006717926.1:n.*157A>G
XM_011539817.1:c.*157A>G XP_011538119.1:n.*157A>G
NM_002412.5:c.*157A>G MANE Select NP_002403.3:n.*157A>G
XM_017016275.1:c.*157A>G XP_016871764.1:n.*157A>G
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