Canonical Allele Identifier: CA596928943
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1419757661
gnomAD v2: 10-131265455-T-C
gnomAD v3: 10-129467191-T-C
gnomAD v4: 10-129467191-T-C
MyVariant Identifiers: chr10:g.131265455T>C (hg19) chr10:g.129467191T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467191T>C , CM000672.2:g.129467191T>C GRCh38
NC_000010.10:g.131265455T>C , CM000672.1:g.131265455T>C GRCh37
NC_000010.9:g.131155445T>C NCBI36
NG_052673.1:g.5008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.-25T>C ENSP00000302111.7:n.-25T>C
ENST00000306010.7:c.-25T>C ENSP00000302111.7:n.-25T>C
NM_002412.3:c.-25T>C NP_002403.2:n.-25T>C
NM_002412.4:c.-25T>C NP_002403.2:n.-25T>C
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