Canonical Allele Identifier: CA1944891572

Gene: MGMT

Linked Data

• dbSNP Id: rs1848948486

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767147T>G , CM000672.2:g.129767147T>G	GRCh38
NC_000010.10:g.131565411T>G , CM000672.1:g.131565411T>G	GRCh37
NC_000010.9:g.131455401T>G	NCBI36
NG_052673.1:g.304964T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*150T>G	ENSP00000302111.7:n.*150T>G
ENST00000651593.1:c.*150T>G MANE Select	ENSP00000498729.1:n.*150T>G
ENST00000306010.7:c.*150T>G	ENSP00000302111.7:n.*150T>G
NM_002412.3:c.*150T>G	NP_002403.2:n.*150T>G
NM_002412.4:c.*150T>G	NP_002403.2:n.*150T>G
XM_006717863.2:c.*150T>G	XP_006717926.1:n.*150T>G
XM_011539817.1:c.*150T>G	XP_011538119.1:n.*150T>G
NM_002412.5:c.*150T>G MANE Select	NP_002403.3:n.*150T>G
XM_017016275.1:c.*150T>G	XP_016871764.1:n.*150T>G