Linked Data
dbSNP Id:
rs1055259
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109734239T>G , CM000663.2:g.109734239T>G | GRCh38 |
| NC_000001.10:g.110276861T>G , CM000663.1:g.110276861T>G | GRCh37 |
| NC_000001.9:g.110078384T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361066.7:c.*2832A>C (GSTM3) MANE Select | ENSP00000354357.2:n.*2832A>C | |
| ENST00000256594.7:c.*2832A>C (GSTM3) | ENSP00000256594.3:n.*2832A>C | |
| ENST00000429410.2:n.82+21891T>G (GSTM5) | ||
| NM_000849.4:c.*2832A>C (GSTM3) | NP_000840.2:n.*2832A>C | |
| NR_024537.1:n.3744A>C (GSTM3) | ||
| NM_000849.5:c.*2832A>C (GSTM3) MANE Select | NP_000840.2:n.*2832A>C | |
| NR_024537.2:n.3744A>C (GSTM3) |