Canonical Allele Identifier: CA216020347
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1803965

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129707928C>A , CM000672.2:g.129707928C>A GRCh38
NC_000010.10:g.131506192C>A , CM000672.1:g.131506192C>A GRCh37
NC_000010.9:g.131396182C>A NCBI36
NG_052673.1:g.245745C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.252C>A ENSP00000302111.7:p.Leu84=
ENST00000651593.1:c.159C>A MANE Select ENSP00000498729.1:p.Leu53=
ENST00000306010.7:c.252C>A ENSP00000302111.7:p.Leu84=
ENST00000462672.1:n.320C>A
NM_002412.3:c.252C>A NP_002403.2:p.Leu84=
NM_002412.4:c.252C>A NP_002403.2:p.Leu84=
XM_005252682.2:c.159C>A XP_005252739.1:p.Leu53=
XM_006717863.2:c.-19C>A XP_006717926.1:n.-19C>A
XM_011539817.1:c.168C>A XP_011538119.1:p.Leu56=
NM_002412.5:c.159C>A MANE Select NP_002403.3:p.Leu53=
XM_017016275.1:c.-19C>A XP_016871764.1:n.-19C>A