Canonical Allele Identifier: CA13175349
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs7922405
gnomAD v2: 10-131509681-G-A
gnomAD v3: 10-129711417-G-A
gnomAD v4: 10-129711417-G-A
MyVariant Identifiers: chr10:g.131509681G>A (hg19) chr10:g.129711417G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129711417G>A , CM000672.2:g.129711417G>A GRCh38
NC_000010.10:g.131509681G>A , CM000672.1:g.131509681G>A GRCh37
NC_000010.9:g.131399671G>A NCBI36
NG_052673.1:g.249234G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.367+3374G>A ENSP00000302111.7:n.367+3374G>A
ENST00000651593.1:c.274+3374G>A MANE Select ENSP00000498729.1:n.274+3374G>A
ENST00000306010.7:c.367+3374G>A ENSP00000302111.7:n.367+3374G>A
ENST00000462672.1:n.435+3374G>A
NM_002412.3:c.367+3374G>A NP_002403.2:n.367+3374G>A
NM_002412.4:c.367+3374G>A NP_002403.2:n.367+3374G>A
XM_005252682.2:c.274+3374G>A XP_005252739.1:n.274+3374G>A
XM_006717863.2:c.97+3374G>A XP_006717926.1:n.97+3374G>A
XM_011539817.1:c.283+3374G>A XP_011538119.1:n.283+3374G>A
NM_002412.5:c.274+3374G>A MANE Select NP_002403.3:n.274+3374G>A
XM_017016275.1:c.97+3374G>A XP_016871764.1:n.97+3374G>A
XR_946467.2:n.3368G>A
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