Canonical Allele Identifier: CA1944760488

Gene: MGMT

Linked Data

• dbSNP Id: rs1845191249

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468148A>G , CM000672.2:g.129468148A>G	GRCh38
NC_000010.10:g.131266412A>G , CM000672.1:g.131266412A>G	GRCh37
NC_000010.9:g.131156402A>G	NCBI36
NG_052673.1:g.5965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+852A>G	ENSP00000302111.7:n.81+852A>G
ENST00000651593.1:c.-13+852A>G MANE Select	ENSP00000498729.1:n.-13+852A>G
ENST00000306010.7:c.81+852A>G	ENSP00000302111.7:n.81+852A>G
ENST00000482547.1:n.35+852A>G
ENST00000482653.1:n.68+852A>G
NM_002412.3:c.81+852A>G	NP_002403.2:n.81+852A>G
NM_002412.4:c.81+852A>G	NP_002403.2:n.81+852A>G
XM_005252682.2:c.-13+707A>G	XP_005252739.1:n.-13+707A>G
NM_002412.5:c.-13+852A>G MANE Select	NP_002403.3:n.-13+852A>G