Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27174938T= , CM000669.2:g.27174938T= | GRCh38 |
| NC_000007.13:g.27214557T= , CM000669.1:g.27214557T= | GRCh37 |
| NC_000007.12:g.27181082T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396344.4:c.11-2765A= (HOXA10) | ENSP00000379633.4:n.11-2765A= | |
| ENST00000465941.1:n.243A= (HOXA9) | ||
| ENST00000470747.4:c.10+4708A= | ENSP00000421799.3:n.10+4708A= | |
| NR_037939.1:n.617-2765A= (HOXA10) | ||
| NR_037940.1:n.616+4708A= | ||
| NR_037939.2:n.217-2765A= (HOXA10) |