Canonical Allele Identifier: CA661615931

Gene: MGMT

Linked Data

• dbSNP Id: rs1211715766
• MyVariant Identifiers: chr10:g.131426068A>G (hg19) ; chr10:g.129627804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129627804A>G , CM000672.2:g.129627804A>G	GRCh38
NC_000010.10:g.131426068A>G , CM000672.1:g.131426068A>G	GRCh37
NC_000010.9:g.131316058A>G	NCBI36
NG_052673.1:g.165621A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000306010.8:c.219-80091A>G	ENSP00000302111.7:n.219-80091A>G
ENST00000651593.1:c.126-80091A>G MANE Select	ENSP00000498729.1:n.126-80091A>G
ENST00000306010.7:c.219-80091A>G	ENSP00000302111.7:n.219-80091A>G
NM_002412.3:c.219-80091A>G	NP_002403.2:n.219-80091A>G
NM_002412.4:c.219-80091A>G	NP_002403.2:n.219-80091A>G
XM_005252682.2:c.126-80091A>G	XP_005252739.1:n.126-80091A>G
XM_006717863.2:c.-125-18958A>G	XP_006717926.1:n.-125-18958A>G
XM_011539817.1:c.-3-18958A>G	XP_011538119.1:n.-3-18958A>G
NM_002412.5:c.126-80091A>G MANE Select	NP_002403.3:n.126-80091A>G