Canonical Allele Identifier: CA597012181

Gene: MGMT

Linked Data

• dbSNP Id: rs1173620611
• gnomAD v2: 10-131565038-C-T
• gnomAD v3: 10-129766774-C-T
• gnomAD v4: 10-129766774-C-T
• MyVariant Identifiers: chr10:g.131565038C>T (hg19) ; chr10:g.129766774C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766774C>T , CM000672.2:g.129766774C>T	GRCh38
NC_000010.10:g.131565038C>T , CM000672.1:g.131565038C>T	GRCh37
NC_000010.9:g.131455028C>T	NCBI36
NG_052673.1:g.304591C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.508-14C>T	ENSP00000302111.7:n.508-14C>T
ENST00000651593.1:c.415-14C>T MANE Select	ENSP00000498729.1:n.415-14C>T
ENST00000306010.7:c.508-14C>T	ENSP00000302111.7:n.508-14C>T
NM_002412.3:c.508-14C>T	NP_002403.2:n.508-14C>T
NM_002412.4:c.508-14C>T	NP_002403.2:n.508-14C>T
XM_005252682.2:c.415-14C>T	XP_005252739.1:n.415-14C>T
XM_006717863.2:c.238-14C>T	XP_006717926.1:n.238-14C>T
XM_011539817.1:c.424-14C>T	XP_011538119.1:n.424-14C>T
NM_002412.5:c.415-14C>T MANE Select	NP_002403.3:n.415-14C>T
XM_017016275.1:c.238-14C>T	XP_016871764.1:n.238-14C>T