Canonical Allele Identifier: CA1944822494
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1847167277

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129627769C>A , CM000672.2:g.129627769C>A GRCh38
NC_000010.10:g.131426033C>A , CM000672.1:g.131426033C>A GRCh37
NC_000010.9:g.131316023C>A NCBI36
NG_052673.1:g.165586C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.219-80126C>A ENSP00000302111.7:n.219-80126C>A
ENST00000651593.1:c.126-80126C>A MANE Select ENSP00000498729.1:n.126-80126C>A
ENST00000306010.7:c.219-80126C>A ENSP00000302111.7:n.219-80126C>A
NM_002412.3:c.219-80126C>A NP_002403.2:n.219-80126C>A
NM_002412.4:c.219-80126C>A NP_002403.2:n.219-80126C>A
XM_005252682.2:c.126-80126C>A XP_005252739.1:n.126-80126C>A
XM_006717863.2:c.-125-18993C>A XP_006717926.1:n.-125-18993C>A
XM_011539817.1:c.-3-18993C>A XP_011538119.1:n.-3-18993C>A
NM_002412.5:c.126-80126C>A MANE Select NP_002403.3:n.126-80126C>A