Linked Data
MyVariant Identifiers:
chr7:g.73097571C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683241C>T , CM000669.2:g.73683241C>T | GRCh38 |
| NC_000007.13:g.73097571C>T , CM000669.1:g.73097571C>T | GRCh37 |
| NC_000007.12:g.72735507C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395176.3:c.183G>A (DNAJC30) MANE Select | ENSP00000378605.1:p.Thr61= | |
| ENST00000395176.2:c.183G>A (DNAJC30) | ENSP00000378605.1:p.Thr61= | |
| ENST00000464615.1:n.217C>T (BUD23) | ||
| NM_032317.2:c.183G>A (DNAJC30) | NP_115693.2:p.Thr61= | |
| NM_032317.3:c.183G>A (DNAJC30) MANE Select | NP_115693.2:p.Thr61= |