Linked Data
dbSNP Id:
rs762077394
ExAC:
1:110279736 A / G
gnomAD v2:
1-110279736-A-G
gnomAD v4:
1-109737114-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737114A>G , CM000663.2:g.109737114A>G | GRCh38 |
| NC_000001.10:g.110279736A>G , CM000663.1:g.110279736A>G | GRCh37 |
| NC_000001.9:g.110081259A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.635T>C (GSTM3) MANE Select | ENSP00000354357.2:p.Ile212Thr | |
| ENST00000256594.7:c.635T>C (GSTM3) | ENSP00000256594.3:p.Ile212Thr | |
| ENST00000361066.6:c.635T>C (GSTM3) | ENSP00000354357.2:p.Ile212Thr | |
| ENST00000429410.2:n.82+24766A>G (GSTM5) | ||
| ENST00000476321.5:n.603T>C (GSTM3) | ||
| ENST00000486823.5:n.599T>C (GSTM3) | ||
| ENST00000488824.1:n.980T>C (GSTM3) | ||
| NM_000849.4:c.635T>C (GSTM3) | NP_000840.2:p.Ile212Thr | |
| NR_024537.1:n.869T>C (GSTM3) | ||
| XM_011541296.1:c.854T>C (GSTM3) | XP_011539598.1:p.Ile285Thr | |
| NM_000849.5:c.635T>C (GSTM3) MANE Select | NP_000840.2:p.Ile212Thr | |
| NR_024537.2:n.869T>C (GSTM3) |