Canonical Allele Identifier: CA1944760544
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1845192668
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129468247A>T , CM000672.2:g.129468247A>T GRCh38
NC_000010.10:g.131266511A>T , CM000672.1:g.131266511A>T GRCh37
NC_000010.9:g.131156501A>T NCBI36
NG_052673.1:g.6064A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.81+951A>T ENSP00000302111.7:n.81+951A>T
ENST00000651593.1:c.-13+951A>T MANE Select ENSP00000498729.1:n.-13+951A>T
ENST00000306010.7:c.81+951A>T ENSP00000302111.7:n.81+951A>T
ENST00000482547.1:n.35+951A>T
ENST00000482653.1:n.68+951A>T
NM_002412.3:c.81+951A>T NP_002403.2:n.81+951A>T
NM_002412.4:c.81+951A>T NP_002403.2:n.81+951A>T
XM_005252682.2:c.-13+806A>T XP_005252739.1:n.-13+806A>T
NM_002412.5:c.-13+951A>T MANE Select NP_002403.3:n.-13+951A>T
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