Canonical Allele Identifier: CA2722838238

Gene: MGMT

Linked Data

• dbSNP Id: rs2119605316

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468171T>C , CM000672.2:g.129468171T>C	GRCh38
NC_000010.10:g.131266435T>C , CM000672.1:g.131266435T>C	GRCh37
NC_000010.9:g.131156425T>C	NCBI36
NG_052673.1:g.5988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+875T>C	ENSP00000302111.7:n.81+875T>C
ENST00000651593.1:c.-13+875T>C MANE Select	ENSP00000498729.1:n.-13+875T>C
ENST00000306010.7:c.81+875T>C	ENSP00000302111.7:n.81+875T>C
ENST00000482547.1:n.35+875T>C
ENST00000482653.1:n.68+875T>C
NM_002412.3:c.81+875T>C	NP_002403.2:n.81+875T>C
NM_002412.4:c.81+875T>C	NP_002403.2:n.81+875T>C
XM_005252682.2:c.-13+730T>C	XP_005252739.1:n.-13+730T>C
NM_002412.5:c.-13+875T>C MANE Select	NP_002403.3:n.-13+875T>C