Linked Data
dbSNP Id:
rs1206052920
gnomAD v2:
1-110279730-T-C
gnomAD v3:
1-109737108-T-C
gnomAD v4:
1-109737108-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737108T>C , CM000663.2:g.109737108T>C | GRCh38 |
| NC_000001.10:g.110279730T>C , CM000663.1:g.110279730T>C | GRCh37 |
| NC_000001.9:g.110081253T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.641A>G (GSTM3) MANE Select | ENSP00000354357.2:p.Asn214Ser | |
| ENST00000256594.7:c.641A>G (GSTM3) | ENSP00000256594.3:p.Asn214Ser | |
| ENST00000361066.6:c.641A>G (GSTM3) | ENSP00000354357.2:p.Asn214Ser | |
| ENST00000429410.2:n.82+24760T>C (GSTM5) | ||
| ENST00000476321.5:n.609A>G (GSTM3) | ||
| ENST00000486823.5:n.605A>G (GSTM3) | ||
| ENST00000488824.1:n.986A>G (GSTM3) | ||
| NM_000849.4:c.641A>G (GSTM3) | NP_000840.2:p.Asn214Ser | |
| NR_024537.1:n.875A>G (GSTM3) | ||
| XM_011541296.1:c.860A>G (GSTM3) | XP_011539598.1:p.Asn287Ser | |
| NM_000849.5:c.641A>G (GSTM3) MANE Select | NP_000840.2:p.Asn214Ser | |
| NR_024537.2:n.875A>G (GSTM3) |