Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.53939296C>G , CM000674.2:g.53939296C>G | GRCh38 |
| NC_000012.11:g.54333080C>G , CM000674.1:g.54333080C>G | GRCh37 |
| NC_000012.10:g.52619347C>G | NCBI36 |
| NG_033026.1:g.5505C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017410.3:c.390C>G (HOXC13) MANE Select | NP_059106.2:p.Tyr130Ter |
| ENST00000243056.5:c.390C>G (HOXC13) MANE Select | ENSP00000243056.3:p.Tyr130Ter |
| NM_017410.2:c.390C>G (HOXC13) | NP_059106.2:p.Tyr130Ter |
| NR_047507.1:n.173+175G>C (HOXC13-AS) | |
| ENST00000243056.4:c.390C>G (HOXC13) | ENSP00000243056.3:p.Tyr130Ter |