Canonical Allele Identifier: CA471816647

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565219A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766955A>C , CM000672.2:g.129766955A>C	GRCh38
NC_000010.10:g.131565219A>C , CM000672.1:g.131565219A>C	GRCh37
NC_000010.9:g.131455209A>C	NCBI36
NG_052673.1:g.304772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.675A>C	ENSP00000302111.7:p.Gly225=
ENST00000651593.1:c.582A>C MANE Select	ENSP00000498729.1:p.Gly194=
ENST00000306010.7:c.675A>C	ENSP00000302111.7:p.Gly225=
NM_002412.3:c.675A>C	NP_002403.2:p.Gly225=
NM_002412.4:c.675A>C	NP_002403.2:p.Gly225=
XM_005252682.2:c.582A>C	XP_005252739.1:p.Gly194=
XM_006717863.2:c.405A>C	XP_006717926.1:p.Gly135=
XM_011539817.1:c.591A>C	XP_011538119.1:p.Gly197=
NM_002412.5:c.582A>C MANE Select	NP_002403.3:p.Gly194=
XM_017016275.1:c.405A>C	XP_016871764.1:p.Gly135=