Canonical Allele Identifier: CA378713126

Gene: MGMT

Linked Data

• dbSNP Id: rs1267918510
• gnomAD v2: 10-131565149-A-C
• gnomAD v4: 10-129766885-A-C
• MyVariant Identifiers: chr10:g.131565149A>C (hg19) ; chr10:g.129766885A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766885A>C , CM000672.2:g.129766885A>C	GRCh38
NC_000010.10:g.131565149A>C , CM000672.1:g.131565149A>C	GRCh37
NC_000010.9:g.131455139A>C	NCBI36
NG_052673.1:g.304702A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.605A>C	ENSP00000302111.7:p.His202Pro
ENST00000651593.1:c.512A>C MANE Select	ENSP00000498729.1:p.His171Pro
ENST00000306010.7:c.605A>C	ENSP00000302111.7:p.His202Pro
NM_002412.3:c.605A>C	NP_002403.2:p.His202Pro
NM_002412.4:c.605A>C	NP_002403.2:p.His202Pro
XM_005252682.2:c.512A>C	XP_005252739.1:p.His171Pro
XM_006717863.2:c.335A>C	XP_006717926.1:p.His112Pro
XM_011539817.1:c.521A>C	XP_011538119.1:p.His174Pro
NM_002412.5:c.512A>C MANE Select	NP_002403.3:p.His171Pro
XM_017016275.1:c.335A>C	XP_016871764.1:p.His112Pro