Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.97006272C>T , CM000669.2:g.97006272C>T | GRCh38 |
| NC_000007.13:g.96635584C>T , CM000669.1:g.96635584C>T | GRCh37 |
| NC_000007.12:g.96473520C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518156.3:c.295C>T (DLX6) MANE Select | ENSP00000428480.2:p.Pro99Ser | |
| ENST00000518156.2:c.295C>T (DLX6) | ENSP00000428480.2:p.Pro99Ser | |
| NM_005222.3:c.295C>T (DLX6) | NP_005213.3:p.Pro99Ser | |
| NR_015448.1:n.141+7653G>A (DLX6-AS1) | ||
| NM_005222.4:c.295C>T (DLX6) MANE Select | NP_005213.3:p.Pro99Ser |