Linked Data
MyVariant Identifiers:
chr17:g.7989335T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8086017T>C , CM000679.2:g.8086017T>C | GRCh38 |
| NC_000017.10:g.7989335T>C , CM000679.1:g.7989335T>C | GRCh37 |
| NC_000017.9:g.7930060T>C | NCBI36 |
| NG_007099.1:g.6687A>G | |
| NG_007099.2:g.6700A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.351A>G MANE Select | ENSP00000497784.1:p.Thr117= | |
| ENST00000319144.4:c.351A>G | ENSP00000315167.4:p.Thr117= | |
| NM_001139.2:c.351A>G | NP_001130.1:p.Thr117= | |
| NM_001139.3:c.351A>G MANE Select | NP_001130.1:p.Thr117= |