Linked Data
MyVariant Identifiers:
chr17:g.39742733G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586481G>C , CM000679.2:g.41586481G>C | GRCh38 |
| NC_000017.10:g.39742733G>C , CM000679.1:g.39742733G>C | GRCh37 |
| NC_000017.9:g.36996259G>C | NCBI36 |
| NG_008624.1:g.5415C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000167586.7:c.354C>G MANE Select | ENSP00000167586.6:p.Thr118= | |
| ENST00000167586.6:c.354C>G | ENSP00000167586.6:p.Thr118= | |
| NM_000526.4:c.354C>G | NP_000517.2:p.Thr118= | |
| NM_000526.5:c.354C>G MANE Select | NP_000517.3:p.Thr118= |