Canonical Allele Identifier: CA378909649
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129467286-T-C
MyVariant Identifiers: chr10:g.131265550T>C (hg19) chr10:g.129467286T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467286T>C , CM000672.2:g.129467286T>C GRCh38
NC_000010.10:g.131265550T>C , CM000672.1:g.131265550T>C GRCh37
NC_000010.9:g.131155540T>C NCBI36
NG_052673.1:g.5103T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.71T>C ENSP00000302111.7:p.Val24Ala
ENST00000651593.1:c.-23T>C MANE Select ENSP00000498729.1:n.-23T>C
ENST00000306010.7:c.71T>C ENSP00000302111.7:p.Val24Ala
ENST00000482547.1:n.25T>C
ENST00000482653.1:n.58T>C
NM_002412.3:c.71T>C NP_002403.2:p.Val24Ala
NM_002412.4:c.71T>C NP_002403.2:p.Val24Ala
NM_002412.5:c.-23T>C MANE Select NP_002403.3:n.-23T>C
Search 100 bp 5'
Search 100 bp 3'