Canonical Allele Identifier: CA471931546
Gene: MGMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.131265551T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467287T>G , CM000672.2:g.129467287T>G GRCh38
NC_000010.10:g.131265551T>G , CM000672.1:g.131265551T>G GRCh37
NC_000010.9:g.131155541T>G NCBI36
NG_052673.1:g.5104T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.72T>G ENSP00000302111.7:p.Val24=
ENST00000651593.1:c.-22T>G MANE Select ENSP00000498729.1:n.-22T>G
ENST00000306010.7:c.72T>G ENSP00000302111.7:p.Val24=
ENST00000482547.1:n.26T>G
ENST00000482653.1:n.59T>G
NM_002412.3:c.72T>G NP_002403.2:p.Val24=
NM_002412.4:c.72T>G NP_002403.2:p.Val24=
NM_002412.5:c.-22T>G MANE Select NP_002403.3:n.-22T>G