Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683131T>G , CM000669.2:g.73683131T>G | GRCh38 |
| NC_000007.13:g.73097461T>G , CM000669.1:g.73097461T>G | GRCh37 |
| NC_000007.12:g.72735397T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032317.3:c.293A>C (DNAJC30) MANE Select | NP_115693.2:p.Tyr98Ser |
| ENST00000395176.3:c.293A>C (DNAJC30) MANE Select | ENSP00000378605.1:p.Tyr98Ser |
| NM_032317.2:c.293A>C (DNAJC30) | NP_115693.2:p.Tyr98Ser |
| ENST00000395176.2:c.293A>C (DNAJC30) | ENSP00000378605.1:p.Tyr98Ser |
| ENST00000464615.1:n.107T>G (BUD23) |