Canonical Allele Identifier: CA2611438418
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129767149-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767149A>C , CM000672.2:g.129767149A>C GRCh38
NC_000010.10:g.131565413A>C , CM000672.1:g.131565413A>C GRCh37
NC_000010.9:g.131455403A>C NCBI36
NG_052673.1:g.304966A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*152A>C ENSP00000302111.7:n.*152A>C
ENST00000651593.1:c.*152A>C MANE Select ENSP00000498729.1:n.*152A>C
ENST00000306010.7:c.*152A>C ENSP00000302111.7:n.*152A>C
NM_002412.3:c.*152A>C NP_002403.2:n.*152A>C
NM_002412.4:c.*152A>C NP_002403.2:n.*152A>C
XM_006717863.2:c.*152A>C XP_006717926.1:n.*152A>C
XM_011539817.1:c.*152A>C XP_011538119.1:n.*152A>C
NM_002412.5:c.*152A>C MANE Select NP_002403.3:n.*152A>C
XM_017016275.1:c.*152A>C XP_016871764.1:n.*152A>C
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