Linked Data
dbSNP Id:
rs146798068
ExAC:
1:110279786 C / T
gnomAD v2:
1-110279786-C-T
gnomAD v3:
1-109737164-C-T
gnomAD v4:
1-109737164-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737164C>T , CM000663.2:g.109737164C>T | GRCh38 |
| NC_000001.10:g.110279786C>T , CM000663.1:g.110279786C>T | GRCh37 |
| NC_000001.9:g.110081309C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.585G>A (GSTM3) MANE Select | ENSP00000354357.2:p.Leu195= | |
| ENST00000256594.7:c.585G>A (GSTM3) | ENSP00000256594.3:p.Leu195= | |
| ENST00000361066.6:c.585G>A (GSTM3) | ENSP00000354357.2:p.Leu195= | |
| ENST00000429410.2:n.82+24816C>T (GSTM5) | ||
| ENST00000476321.5:n.553G>A (GSTM3) | ||
| ENST00000486823.5:n.549G>A (GSTM3) | ||
| ENST00000488824.1:n.930G>A (GSTM3) | ||
| NM_000849.4:c.585G>A (GSTM3) | NP_000840.2:p.Leu195= | |
| NR_024537.1:n.819G>A (GSTM3) | ||
| XM_011541296.1:c.804G>A (GSTM3) | XP_011539598.1:p.Leu268= | |
| NM_000849.5:c.585G>A (GSTM3) MANE Select | NP_000840.2:p.Leu195= | |
| NR_024537.2:n.819G>A (GSTM3) |