Canonical Allele Identifier: CA471816664

Gene: MGMT

Linked Data

• dbSNP Id: rs764371384
• MyVariant Identifiers: chr10:g.131565234G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766970G>T , CM000672.2:g.129766970G>T	GRCh38
NC_000010.10:g.131565234G>T , CM000672.1:g.131565234G>T	GRCh37
NC_000010.9:g.131455224G>T	NCBI36
NG_052673.1:g.304787G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.690G>T	ENSP00000302111.7:p.Ser230=
ENST00000651593.1:c.597G>T MANE Select	ENSP00000498729.1:p.Ser199=
ENST00000306010.7:c.690G>T	ENSP00000302111.7:p.Ser230=
NM_002412.3:c.690G>T	NP_002403.2:p.Ser230=
NM_002412.4:c.690G>T	NP_002403.2:p.Ser230=
XM_005252682.2:c.597G>T	XP_005252739.1:p.Ser199=
XM_006717863.2:c.420G>T	XP_006717926.1:p.Ser140=
XM_011539817.1:c.606G>T	XP_011538119.1:p.Ser202=
NM_002412.5:c.597G>T MANE Select	NP_002403.3:p.Ser199=
XM_017016275.1:c.420G>T	XP_016871764.1:p.Ser140=