Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.214593T>C , CM000671.2:g.214593T>C | GRCh38 |
| NC_000009.11:g.214593T>C , CM000671.1:g.214593T>C | GRCh37 |
| NC_000009.10:g.204593T>C | NCBI36 |
| NG_017007.1:g.4729T>C , LRG_196:g.4729T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_152569.2:c.804A>G (DOCK8-AS1) | NP_689782.2:p.Glu268= |
| NR_160804.1:n.1158A>G (DOCK8-AS1) | |
| ENST00000382387.3:c.804A>G (DOCK8-AS1) | ENSP00000371824.2:p.Glu268= |
| XM_011518045.3:c.-152+3277T>C (DOCK8) | XP_011516347.1:n.-152+3277T>C |
| XM_017015173.1:c.-152+3277T>C (DOCK8) | XP_016870662.1:n.-152+3277T>C |