Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176153998T>C , CM000664.2:g.176153998T>C | GRCh38 |
| NC_000002.11:g.177018726T>C , CM000664.1:g.177018726T>C | GRCh37 |
| NC_000002.10:g.176726972T>C | NCBI36 |
| NG_012080.1:g.7614T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000432796.2:c.-84-15033T>C (HOXD3) | ENSP00000392615.2:n.-84-15033T>C |
| ENST00000468418.4:c.*325+961T>C | ENSP00000424734.3:n.*325+961T>C |
| XM_005246510.3:c.-180-10075T>C (HOXD3) | XP_005246567.1:n.-180-10075T>C |
| XM_005246514.4:c.*1286T>C (HOXD4) | XP_005246571.1:n.*1286T>C |
| XM_006712477.2:c.-84-15033T>C (HOXD3) | XP_006712540.1:n.-84-15033T>C |