Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945951A= , CM000665.2:g.138945951A= | GRCh38 |
| NC_000003.11:g.138664793A= , CM000665.1:g.138664793A= | GRCh37 |
| NC_000003.10:g.140147483A= | NCBI36 |
| NG_012454.1:g.6190T= | |
| NG_029796.1:g.3718A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_023067.4:c.772T= MANE Select | NP_075555.1:p.Tyr258= |
| ENST00000648323.1:c.772T= MANE Select | ENSP00000497217.1:p.Tyr258= |
| NM_023067.3:c.772T= | NP_075555.1:p.Tyr258= |
| ENST00000330315.3:c.772T= | ENSP00000333188.3:p.Tyr258= |