Canonical Allele Identifier: CA378713332

Gene: MGMT

Linked Data

• dbSNP Id: rs1848946387
• gnomAD v4: 10-129766995-T-C
• MyVariant Identifiers: chr10:g.131565259T>C (hg19) ; chr10:g.129766995T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766995T>C , CM000672.2:g.129766995T>C	GRCh38
NC_000010.10:g.131565259T>C , CM000672.1:g.131565259T>C	GRCh37
NC_000010.9:g.131455249T>C	NCBI36
NG_052673.1:g.304812T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.715T>C	ENSP00000302111.7:p.Ter239Arg
ENST00000651593.1:c.622T>C MANE Select	ENSP00000498729.1:p.Ter208Arg
ENST00000306010.7:c.715T>C	ENSP00000302111.7:p.Ter239Arg
NM_002412.3:c.715T>C	NP_002403.2:p.Ter239Arg
NM_002412.4:c.715T>C	NP_002403.2:p.Ter239Arg
XM_005252682.2:c.622T>C	XP_005252739.1:p.Ter208Arg
XM_006717863.2:c.445T>C	XP_006717926.1:p.Ter149Arg
XM_011539817.1:c.631T>C	XP_011538119.1:p.Ter211Arg
NM_002412.5:c.622T>C MANE Select	NP_002403.3:p.Ter208Arg
XM_017016275.1:c.445T>C	XP_016871764.1:p.Ter149Arg