Canonical Allele Identifier: CA2722674663
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1369295071

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767174A>G , CM000672.2:g.129767174A>G GRCh38
NC_000010.10:g.131565438A>G , CM000672.1:g.131565438A>G GRCh37
NC_000010.9:g.131455428A>G NCBI36
NG_052673.1:g.304991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*177A>G ENSP00000302111.7:n.*177A>G
ENST00000651593.1:c.*177A>G MANE Select ENSP00000498729.1:n.*177A>G
ENST00000306010.7:c.*177A>G ENSP00000302111.7:n.*177A>G
NM_002412.3:c.*177A>G NP_002403.2:n.*177A>G
NM_002412.4:c.*177A>G NP_002403.2:n.*177A>G
XM_006717863.2:c.*177A>G XP_006717926.1:n.*177A>G
XM_011539817.1:c.*177A>G XP_011538119.1:n.*177A>G
NM_002412.5:c.*177A>G MANE Select NP_002403.3:n.*177A>G
XM_017016275.1:c.*177A>G XP_016871764.1:n.*177A>G