Canonical Allele Identifier: CA661560487

Gene: MGMT

Linked Data

• dbSNP Id: rs1220781025
• gnomAD v3: 10-129468333-C-T
• gnomAD v4: 10-129468333-C-T
• MyVariant Identifiers: chr10:g.131266597C>T (hg19) ; chr10:g.129468333C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468333C>T , CM000672.2:g.129468333C>T	GRCh38
NC_000010.10:g.131266597C>T , CM000672.1:g.131266597C>T	GRCh37
NC_000010.9:g.131156587C>T	NCBI36
NG_052673.1:g.6150C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+1037C>T	ENSP00000302111.7:n.81+1037C>T
ENST00000651593.1:c.-13+1037C>T MANE Select	ENSP00000498729.1:n.-13+1037C>T
ENST00000306010.7:c.81+1037C>T	ENSP00000302111.7:n.81+1037C>T
ENST00000482547.1:n.35+1037C>T
ENST00000482653.1:n.68+1037C>T
NM_002412.3:c.81+1037C>T	NP_002403.2:n.81+1037C>T
NM_002412.4:c.81+1037C>T	NP_002403.2:n.81+1037C>T
XM_005252682.2:c.-13+892C>T	XP_005252739.1:n.-13+892C>T
NM_002412.5:c.-13+1037C>T MANE Select	NP_002403.3:n.-13+1037C>T