Canonical Allele Identifier: CA378713327

Gene: MGMT

Linked Data

• dbSNP Id: rs1848946294
• gnomAD v4: 10-129766993-A-G
• MyVariant Identifiers: chr10:g.131565257A>G (hg19) ; chr10:g.129766993A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766993A>G , CM000672.2:g.129766993A>G	GRCh38
NC_000010.10:g.131565257A>G , CM000672.1:g.131565257A>G	GRCh37
NC_000010.9:g.131455247A>G	NCBI36
NG_052673.1:g.304810A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.713A>G	ENSP00000302111.7:p.Asn238Ser
ENST00000651593.1:c.620A>G MANE Select	ENSP00000498729.1:p.Asn207Ser
ENST00000306010.7:c.713A>G	ENSP00000302111.7:p.Asn238Ser
NM_002412.3:c.713A>G	NP_002403.2:p.Asn238Ser
NM_002412.4:c.713A>G	NP_002403.2:p.Asn238Ser
XM_005252682.2:c.620A>G	XP_005252739.1:p.Asn207Ser
XM_006717863.2:c.443A>G	XP_006717926.1:p.Asn148Ser
XM_011539817.1:c.629A>G	XP_011538119.1:p.Asn210Ser
NM_002412.5:c.620A>G MANE Select	NP_002403.3:p.Asn207Ser
XM_017016275.1:c.443A>G	XP_016871764.1:p.Asn148Ser