Linked Data
MyVariant Identifiers:
chr1:g.110279570C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109736948C>G , CM000663.2:g.109736948C>G | GRCh38 |
| NC_000001.10:g.110279570C>G , CM000663.1:g.110279570C>G | GRCh37 |
| NC_000001.9:g.110081093C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.*123G>C (GSTM3) MANE Select | ENSP00000354357.2:n.*123G>C | |
| ENST00000256594.7:c.*123G>C (GSTM3) | ENSP00000256594.3:n.*123G>C | |
| ENST00000361066.6:c.*123G>C (GSTM3) | ENSP00000354357.2:n.*123G>C | |
| ENST00000429410.2:n.82+24600C>G (GSTM5) | ||
| ENST00000486823.5:n.765G>C (GSTM3) | ||
| NM_000849.4:c.*123G>C (GSTM3) | NP_000840.2:n.*123G>C | |
| NR_024537.1:n.1035G>C (GSTM3) | ||
| NM_000849.5:c.*123G>C (GSTM3) MANE Select | NP_000840.2:n.*123G>C | |
| NR_024537.2:n.1035G>C (GSTM3) |