Canonical Allele Identifier: CA215499764

Gene: MGMT

Linked Data

• dbSNP Id: rs55800711
• gnomAD v2: 10-131565006-G-A
• gnomAD v4: 10-129766742-G-A
• MyVariant Identifiers: chr10:g.131565006G>A (hg19) ; chr10:g.129766742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766742G>A , CM000672.2:g.129766742G>A	GRCh38
NC_000010.10:g.131565006G>A , CM000672.1:g.131565006G>A	GRCh37
NC_000010.9:g.131454996G>A	NCBI36
NG_052673.1:g.304559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.508-46G>A	ENSP00000302111.7:n.508-46G>A
ENST00000651593.1:c.415-46G>A MANE Select	ENSP00000498729.1:n.415-46G>A
ENST00000306010.7:c.508-46G>A	ENSP00000302111.7:n.508-46G>A
NM_002412.3:c.508-46G>A	NP_002403.2:n.508-46G>A
NM_002412.4:c.508-46G>A	NP_002403.2:n.508-46G>A
XM_005252682.2:c.415-46G>A	XP_005252739.1:n.415-46G>A
XM_006717863.2:c.238-46G>A	XP_006717926.1:n.238-46G>A
XM_011539817.1:c.424-46G>A	XP_011538119.1:n.424-46G>A
NM_002412.5:c.415-46G>A MANE Select	NP_002403.3:n.415-46G>A
XM_017016275.1:c.238-46G>A	XP_016871764.1:n.238-46G>A