Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49634346G>C , CM000676.2:g.49634346G>C | GRCh38 |
| NC_000014.8:g.50101064G>C , CM000676.1:g.50101064G>C | GRCh37 |
| NC_000014.7:g.49170814G>C | NCBI36 |
| NG_013070.1:g.5885C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298292.13:c.804C>G MANE Select | ENSP00000298292.8:p.Tyr268Ter | |
| ENST00000298292.12:c.804C>G | ENSP00000298292.8:p.Tyr268Ter | |
| ENST00000406043.3:c.804C>G | ENSP00000384862.3:p.Tyr268Ter | |
| NM_001083908.1:c.804C>G | NP_001077377.1:p.Tyr268Ter | |
| NM_018139.2:c.804C>G | NP_060609.2:p.Tyr268Ter | |
| NM_001083908.2:c.804C>G | NP_001077377.1:p.Tyr268Ter | |
| NM_018139.3:c.804C>G MANE Select | NP_060609.2:p.Tyr268Ter |