Canonical Allele Identifier: CA215989578

Gene: MGMT

Linked Data

• dbSNP Id: rs572222970
• gnomAD v3: 10-129468233-C-A
• gnomAD v4: 10-129468233-C-A
• MyVariant Identifiers: chr10:g.131266497C>A (hg19) ; chr10:g.129468233C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468233C>A , CM000672.2:g.129468233C>A	GRCh38
NC_000010.10:g.131266497C>A , CM000672.1:g.131266497C>A	GRCh37
NC_000010.9:g.131156487C>A	NCBI36
NG_052673.1:g.6050C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000306010.8:c.81+937C>A	ENSP00000302111.7:n.81+937C>A
ENST00000651593.1:c.-13+937C>A MANE Select	ENSP00000498729.1:n.-13+937C>A
ENST00000306010.7:c.81+937C>A	ENSP00000302111.7:n.81+937C>A
ENST00000482547.1:n.35+937C>A
ENST00000482653.1:n.68+937C>A
NM_002412.3:c.81+937C>A	NP_002403.2:n.81+937C>A
NM_002412.4:c.81+937C>A	NP_002403.2:n.81+937C>A
XM_005252682.2:c.-13+792C>A	XP_005252739.1:n.-13+792C>A
NM_002412.5:c.-13+937C>A MANE Select	NP_002403.3:n.-13+937C>A