Canonical Allele Identifier: CA215989577

Gene: MGMT

Linked Data

• dbSNP Id: rs911477911
• MyVariant Identifiers: chr10:g.131266495G>T (hg19) ; chr10:g.129468231G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468231G>T , CM000672.2:g.129468231G>T	GRCh38
NC_000010.10:g.131266495G>T , CM000672.1:g.131266495G>T	GRCh37
NC_000010.9:g.131156485G>T	NCBI36
NG_052673.1:g.6048G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+935G>T	ENSP00000302111.7:n.81+935G>T
ENST00000651593.1:c.-13+935G>T MANE Select	ENSP00000498729.1:n.-13+935G>T
ENST00000306010.7:c.81+935G>T	ENSP00000302111.7:n.81+935G>T
ENST00000482547.1:n.35+935G>T
ENST00000482653.1:n.68+935G>T
NM_002412.3:c.81+935G>T	NP_002403.2:n.81+935G>T
NM_002412.4:c.81+935G>T	NP_002403.2:n.81+935G>T
XM_005252682.2:c.-13+790G>T	XP_005252739.1:n.-13+790G>T
NM_002412.5:c.-13+935G>T MANE Select	NP_002403.3:n.-13+935G>T