Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8072813G>C , CM000679.2:g.8072813G>C | GRCh38 |
| NC_000017.10:g.7976131G>C , CM000679.1:g.7976131G>C | GRCh37 |
| NC_000017.9:g.7916856G>C | NCBI36 |
| NG_007099.1:g.19891C>G | |
| NG_007099.2:g.19904C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.2064C>G MANE Select | NP_001130.1:p.Tyr688Ter |
| ENST00000647874.1:c.2064C>G MANE Select | ENSP00000497784.1:p.Tyr688Ter |
| NM_001139.2:c.2064C>G | NP_001130.1:p.Tyr688Ter |
| ENST00000319144.4:c.2064C>G | ENSP00000315167.4:p.Tyr688Ter |
| ENST00000649809.1:c.1128C>G | ENSP00000496845.1:p.Tyr376Ter |
| ENST00000650441.1:n.487C>G |