Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109740350G= , CM000663.2:g.109740350G= | GRCh38 |
| NC_000001.10:g.110282972G= , CM000663.1:g.110282972G= | GRCh37 |
| NC_000001.9:g.110084495G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.-63C= (GSTM3) MANE Select | ENSP00000354357.2:n.-63C= | |
| ENST00000256594.7:c.-63C= (GSTM3) | ENSP00000256594.3:n.-63C= | |
| ENST00000361066.6:c.-63C= (GSTM3) | ENSP00000354357.2:n.-63C= | |
| ENST00000429410.2:n.82+28002G= (GSTM5) | ||
| NM_000849.4:c.-63C= (GSTM3) | NP_000840.2:n.-63C= | |
| NR_024537.1:n.248C= (GSTM3) | ||
| XM_011541296.1:c.233C= (GSTM3) | XP_011539598.1:p.Ser78= | |
| NM_000849.5:c.-63C= (GSTM3) MANE Select | NP_000840.2:n.-63C= | |
| NR_024537.2:n.248C= (GSTM3) |