Linked Data
MyVariant Identifiers:
chr17:g.13972725C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.14069408C>G , CM000679.2:g.14069408C>G | GRCh38 |
| NC_000017.10:g.13972725C>G , CM000679.1:g.13972725C>G | GRCh37 |
| NC_000017.9:g.13913450C>G | NCBI36 |
| NG_008034.1:g.5007C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001303.3:c.-198C>G (COX10) | NP_001294.2:n.-198C>G | |
| NR_049718.1:n.51G>C (COX10-DT) |