Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173202G>T , CM000678.2:g.173202G>T | GRCh38 |
| NC_000016.9:g.223201G>T , CM000678.1:g.223201G>T | GRCh37 |
| NC_000016.8:g.163201G>T | NCBI36 |
| NG_000006.1:g.34065G>T | |
| NG_059186.1:g.1552G>T | |
| NG_059271.1:g.5356G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.173G>T MANE Select | ENSP00000251595.6:p.Gly58Val | |
| ENST00000251595.10:c.173G>T | ENSP00000251595.6:p.Gly58Val | |
| ENST00000397806.1:c.77G>T | ENSP00000380908.1:p.Gly26Val | |
| ENST00000482565.1:n.309G>T | ||
| ENST00000484216.1:n.142G>T | ||
| NM_000517.4:c.173G>T | NP_000508.1:p.Gly58Val | |
| NM_000517.6:c.173G>T MANE Select | NP_000508.1:p.Gly58Val |