Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153743496C>T , CM000685.2:g.153743496C>T | GRCh38 |
| NC_000023.10:g.153008950C>T , CM000685.1:g.153008950C>T | GRCh37 |
| NC_000023.9:g.152662144C>T | NCBI36 |
| NG_009022.2:g.23629C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.1999C>T MANE Select | NP_000024.2:p.His667Tyr |
| ENST00000218104.6:c.1999C>T MANE Select | ENSP00000218104.3:p.His667Tyr |
| NM_000033.3:c.1999C>T | NP_000024.2:p.His667Tyr |
| ENST00000218104.5:c.1999C>T | ENSP00000218104.3:p.His667Tyr |
| XR_938507.1:n.2471C>T | |
| XR_938507.2:n.2471C>T |