Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.86567770C>T , CM000678.2:g.86567770C>T | GRCh38 |
| NC_000016.9:g.86601376C>T , CM000678.1:g.86601376C>T | GRCh37 |
| NC_000016.8:g.85158877C>T | NCBI36 |
| NG_012025.1:g.5520C>T | |
| NG_012025.2:g.5942C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649859.1:c.435C>T MANE Select | ENSP00000497759.1:p.Tyr145= | |
| ENST00000320354.5:c.435C>T | ENSP00000326371.4:p.Tyr145= | |
| NM_005251.2:c.435C>T | NP_005242.1:p.Tyr145= | |
| NM_005251.3:c.435C>T MANE Select | NP_005242.1:p.Tyr145= |