Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109734239T= , CM000663.2:g.109734239T= | GRCh38 |
| NC_000001.10:g.110276861T= , CM000663.1:g.110276861T= | GRCh37 |
| NC_000001.9:g.110078384T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000849.5:c.*2832A= (GSTM3) MANE Select | NP_000840.2:n.*2832A= |
| ENST00000361066.7:c.*2832A= (GSTM3) MANE Select | ENSP00000354357.2:n.*2832A= |
| NM_000849.4:c.*2832A= (GSTM3) | NP_000840.2:n.*2832A= |
| NR_024537.1:n.3744A= (GSTM3) | |
| NR_024537.2:n.3744A= (GSTM3) | |
| ENST00000256594.7:c.*2832A= (GSTM3) | ENSP00000256594.3:n.*2832A= |
| ENST00000429410.2:n.82+21891T= (GSTM5) |