Linked Data
dbSNP Id:
rs7483
ExAC:
1:110279701 C / T
gnomAD v2:
1-110279701-C-T
gnomAD v3:
1-109737079-C-T
gnomAD v4:
1-109737079-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737079C>T , CM000663.2:g.109737079C>T | GRCh38 |
| NC_000001.10:g.110279701C>T , CM000663.1:g.110279701C>T | GRCh37 |
| NC_000001.9:g.110081224C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361066.7:c.670G>A (GSTM3) MANE Select | ENSP00000354357.2:p.Val224Ile | |
| ENST00000256594.7:c.670G>A (GSTM3) | ENSP00000256594.3:p.Val224Ile | |
| ENST00000361066.6:c.670G>A (GSTM3) | ENSP00000354357.2:p.Val224Ile | |
| ENST00000429410.2:n.82+24731C>T (GSTM5) | ||
| ENST00000476321.5:n.638G>A (GSTM3) | ||
| ENST00000486823.5:n.634G>A (GSTM3) | ||
| ENST00000488824.1:n.1015G>A (GSTM3) | ||
| NM_000849.4:c.670G>A (GSTM3) | NP_000840.2:p.Val224Ile | |
| NR_024537.1:n.904G>A (GSTM3) | ||
| XM_011541296.1:c.889G>A (GSTM3) | XP_011539598.1:p.Val297Ile | |
| NM_000849.5:c.670G>A (GSTM3) MANE Select | NP_000840.2:p.Val224Ile | |
| NR_024537.2:n.904G>A (GSTM3) |