Canonical Allele Identifier: CA661615926

Gene: MGMT

Linked Data

• dbSNP Id: rs1264149328
• gnomAD v3: 10-129627778-A-C
• gnomAD v4: 10-129627778-A-C
• MyVariant Identifiers: chr10:g.131426042A>C (hg19) ; chr10:g.129627778A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129627778A>C , CM000672.2:g.129627778A>C	GRCh38
NC_000010.10:g.131426042A>C , CM000672.1:g.131426042A>C	GRCh37
NC_000010.9:g.131316032A>C	NCBI36
NG_052673.1:g.165595A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.219-80117A>C	ENSP00000302111.7:n.219-80117A>C
ENST00000651593.1:c.126-80117A>C MANE Select	ENSP00000498729.1:n.126-80117A>C
ENST00000306010.7:c.219-80117A>C	ENSP00000302111.7:n.219-80117A>C
NM_002412.3:c.219-80117A>C	NP_002403.2:n.219-80117A>C
NM_002412.4:c.219-80117A>C	NP_002403.2:n.219-80117A>C
XM_005252682.2:c.126-80117A>C	XP_005252739.1:n.126-80117A>C
XM_006717863.2:c.-125-18984A>C	XP_006717926.1:n.-125-18984A>C
XM_011539817.1:c.-3-18984A>C	XP_011538119.1:n.-3-18984A>C
NM_002412.5:c.126-80117A>C MANE Select	NP_002403.3:n.126-80117A>C