Linked Data
dbSNP Id:
rs1429656435
gnomAD v2:
1-110279754-T-G
gnomAD v3:
1-109737132-T-G
gnomAD v4:
1-109737132-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737132T>G , CM000663.2:g.109737132T>G | GRCh38 |
| NC_000001.10:g.110279754T>G , CM000663.1:g.110279754T>G | GRCh37 |
| NC_000001.9:g.110081277T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.617A>C (GSTM3) MANE Select | ENSP00000354357.2:p.Gln206Pro | |
| ENST00000256594.7:c.617A>C (GSTM3) | ENSP00000256594.3:p.Gln206Pro | |
| ENST00000361066.6:c.617A>C (GSTM3) | ENSP00000354357.2:p.Gln206Pro | |
| ENST00000429410.2:n.82+24784T>G (GSTM5) | ||
| ENST00000476321.5:n.585A>C (GSTM3) | ||
| ENST00000486823.5:n.581A>C (GSTM3) | ||
| ENST00000488824.1:n.962A>C (GSTM3) | ||
| NM_000849.4:c.617A>C (GSTM3) | NP_000840.2:p.Gln206Pro | |
| NR_024537.1:n.851A>C (GSTM3) | ||
| XM_011541296.1:c.836A>C (GSTM3) | XP_011539598.1:p.Gln279Pro | |
| NM_000849.5:c.617A>C (GSTM3) MANE Select | NP_000840.2:p.Gln206Pro | |
| NR_024537.2:n.851A>C (GSTM3) |