Linked Data
MyVariant Identifiers:
chr1:g.110279567A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109736945A>C , CM000663.2:g.109736945A>C | GRCh38 |
| NC_000001.10:g.110279567A>C , CM000663.1:g.110279567A>C | GRCh37 |
| NC_000001.9:g.110081090A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.*126T>G (GSTM3) MANE Select | ENSP00000354357.2:n.*126T>G | |
| ENST00000256594.7:c.*126T>G (GSTM3) | ENSP00000256594.3:n.*126T>G | |
| ENST00000361066.6:c.*126T>G (GSTM3) | ENSP00000354357.2:n.*126T>G | |
| ENST00000429410.2:n.82+24597A>C (GSTM5) | ||
| ENST00000486823.5:n.768T>G (GSTM3) | ||
| NM_000849.4:c.*126T>G (GSTM3) | NP_000840.2:n.*126T>G | |
| NR_024537.1:n.1038T>G (GSTM3) | ||
| NM_000849.5:c.*126T>G (GSTM3) MANE Select | NP_000840.2:n.*126T>G | |
| NR_024537.2:n.1038T>G (GSTM3) |