Canonical Allele Identifier: CA215992025
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs12769288

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129488086C>T , CM000672.2:g.129488086C>T GRCh38
NC_000010.10:g.131286350C>T , CM000672.1:g.131286350C>T GRCh37
NC_000010.9:g.131176340C>T NCBI36
NG_052673.1:g.25903C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.81+20790C>T ENSP00000302111.7:n.81+20790C>T
ENST00000651593.1:c.-13+20790C>T MANE Select ENSP00000498729.1:n.-13+20790C>T
ENST00000306010.7:c.81+20790C>T ENSP00000302111.7:n.81+20790C>T
ENST00000482547.1:n.35+20790C>T
ENST00000482653.1:n.68+20790C>T
NM_002412.3:c.81+20790C>T NP_002403.2:n.81+20790C>T
NM_002412.4:c.81+20790C>T NP_002403.2:n.81+20790C>T
XM_005252682.2:c.-13+20645C>T XP_005252739.1:n.-13+20645C>T
NM_002412.5:c.-13+20790C>T MANE Select NP_002403.3:n.-13+20790C>T