Canonical Allele Identifier: CA216010110

Gene: MGMT

Linked Data

• dbSNP Id: rs1030751629
• gnomAD v3: 10-129627806-A-G
• gnomAD v4: 10-129627806-A-G
• MyVariant Identifiers: chr10:g.131426070A>G (hg19) ; chr10:g.129627806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129627806A>G , CM000672.2:g.129627806A>G	GRCh38
NC_000010.10:g.131426070A>G , CM000672.1:g.131426070A>G	GRCh37
NC_000010.9:g.131316060A>G	NCBI36
NG_052673.1:g.165623A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000306010.8:c.219-80089A>G	ENSP00000302111.7:n.219-80089A>G
ENST00000651593.1:c.126-80089A>G MANE Select	ENSP00000498729.1:n.126-80089A>G
ENST00000306010.7:c.219-80089A>G	ENSP00000302111.7:n.219-80089A>G
NM_002412.3:c.219-80089A>G	NP_002403.2:n.219-80089A>G
NM_002412.4:c.219-80089A>G	NP_002403.2:n.219-80089A>G
XM_005252682.2:c.126-80089A>G	XP_005252739.1:n.126-80089A>G
XM_006717863.2:c.-125-18956A>G	XP_006717926.1:n.-125-18956A>G
XM_011539817.1:c.-3-18956A>G	XP_011538119.1:n.-3-18956A>G
NM_002412.5:c.126-80089A>G MANE Select	NP_002403.3:n.126-80089A>G