Canonical Allele Identifier: CA5748184

Gene: MGMT

Linked Data

• dbSNP Id: rs771718932
• ExAC: 10:131565268 G / A
• gnomAD v2: 10-131565268-G-A
• gnomAD v4: 10-129767004-G-A
• MyVariant Identifiers: chr10:g.131565268G>A (hg19) ; chr10:g.129767004G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767004G>A , CM000672.2:g.129767004G>A	GRCh38
NC_000010.10:g.131565268G>A , CM000672.1:g.131565268G>A	GRCh37
NC_000010.9:g.131455258G>A	NCBI36
NG_052673.1:g.304821G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*7G>A	ENSP00000302111.7:n.*7G>A
ENST00000651593.1:c.*7G>A MANE Select	ENSP00000498729.1:n.*7G>A
ENST00000306010.7:c.*7G>A	ENSP00000302111.7:n.*7G>A
NM_002412.3:c.*7G>A	NP_002403.2:n.*7G>A
NM_002412.4:c.*7G>A	NP_002403.2:n.*7G>A
XM_005252682.2:c.*7G>A	XP_005252739.1:n.*7G>A
XM_006717863.2:c.*7G>A	XP_006717926.1:n.*7G>A
XM_011539817.1:c.*7G>A	XP_011538119.1:n.*7G>A
NM_002412.5:c.*7G>A MANE Select	NP_002403.3:n.*7G>A
XM_017016275.1:c.*7G>A	XP_016871764.1:n.*7G>A