Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.12937202T= , CM000673.2:g.12937202T= | GRCh38 |
| NC_000011.9:g.12958749T= , CM000673.1:g.12958749T= | GRCh37 |
| NC_000011.8:g.12915325T= | NCBI36 |
| NG_021302.1:g.267781T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021961.6:c.1261T= MANE Select | NP_068780.2:p.Tyr421= |
| ENST00000527636.7:c.1261T= MANE Select | ENSP00000435233.2:p.Tyr421= |
| NM_021961.5:c.1261T= | NP_068780.2:p.Tyr421= |
| ENST00000334310.10:c.1054T= | ENSP00000334754.6:p.Tyr352= |
| ENST00000361985.6:c.1066T= | ENSP00000354588.3:p.Tyr356= |
| ENST00000526600.1:c.973T= | ENSP00000435393.1:p.Tyr325= |
| ENST00000527575.5:c.1087T= | ENSP00000435977.1:p.Tyr363= |
| ENST00000527575.6:c.1087T= | ENSP00000435977.2:p.Tyr363= |
| ENST00000527636.5:c.1261T= | ENSP00000435233.1:p.Tyr421= |