gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00002559 (AFR)
Genomes Max Group AF
0.00001059 (NFE)
Exomes Max Group AF
0.000055 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109689155G>T , CM000663.2:g.109689155G>T | GRCh38 |
| NC_000001.10:g.110231777G>T , CM000663.1:g.110231777G>T | GRCh37 |
| NC_000001.9:g.110033300G>T | NCBI36 |
| NG_009246.1:g.6360G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309851.10:c.259+26G>T (GSTM1) MANE Select | ENSP00000311469.5:n.259+26G>T | |
| ENST00000309851.9:c.259+26G>T (GSTM1) | ENSP00000311469.5:n.259+26G>T | |
| ENST00000349334.7:c.259+26G>T (GSTM1) | ENSP00000234981.4:n.259+26G>T | |
| ENST00000369819.2:c.259+26G>T (GSTM1) | ENSP00000358834.2:n.259+26G>T | |
| ENST00000369823.6:c.316+26G>T (GSTM1) | ENSP00000358838.2:n.316+26G>T | |
| ENST00000369831.6:c.567+17572G>T (GSTM2) | ENSP00000358846.2:n.567+17572G>T | |
| ENST00000460717.7:c.*17+7321G>T (GSTM2) | ENSP00000435910.2:n.*17+7321G>T | |
| ENST00000476065.6:c.157+26G>T (GSTM1) | ENSP00000456315.1:n.157+26G>T | |
| ENST00000483399.6:c.178-70G>T (GSTM1) | ENSP00000455929.1:n.178-70G>T | |
| ENST00000490021.2:n.243+26G>T (GSTM1) | ||
| NM_000561.3:c.259+26G>T (GSTM1) | NP_000552.2:n.259+26G>T | |
| NM_146421.2:c.259+26G>T (GSTM1) | NP_666533.1:n.259+26G>T | |
| XM_005270782.3:c.157+26G>T (GSTM1) | XP_005270839.1:n.157+26G>T | |
| XM_005270783.3:c.-53-70G>T (GSTM1) | XP_005270840.1:n.-53-70G>T | |
| XM_005270782.5:c.157+26G>T (GSTM1) | XP_005270839.1:n.157+26G>T | |
| NM_000561.4:c.259+26G>T (GSTM1) MANE Select | NP_000552.2:n.259+26G>T | |
| NM_146421.3:c.259+26G>T (GSTM1) | NP_666533.1:n.259+26G>T |