Canonical Allele Identifier: CA597012188

Gene: MGMT

Linked Data

• dbSNP Id: rs1434055090
• gnomAD v2: 10-131565369-C-T
• gnomAD v3: 10-129767105-C-T
• gnomAD v4: 10-129767105-C-T
• MyVariant Identifiers: chr10:g.131565369C>T (hg19) ; chr10:g.129767105C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767105C>T , CM000672.2:g.129767105C>T	GRCh38
NC_000010.10:g.131565369C>T , CM000672.1:g.131565369C>T	GRCh37
NC_000010.9:g.131455359C>T	NCBI36
NG_052673.1:g.304922C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*108C>T	ENSP00000302111.7:n.*108C>T
ENST00000651593.1:c.*108C>T MANE Select	ENSP00000498729.1:n.*108C>T
ENST00000306010.7:c.*108C>T	ENSP00000302111.7:n.*108C>T
NM_002412.3:c.*108C>T	NP_002403.2:n.*108C>T
NM_002412.4:c.*108C>T	NP_002403.2:n.*108C>T
XM_005252682.2:c.*108C>T	XP_005252739.1:n.*108C>T
XM_006717863.2:c.*108C>T	XP_006717926.1:n.*108C>T
XM_011539817.1:c.*108C>T	XP_011538119.1:n.*108C>T
NM_002412.5:c.*108C>T MANE Select	NP_002403.3:n.*108C>T
XM_017016275.1:c.*108C>T	XP_016871764.1:n.*108C>T