Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.93954075T= , CM000671.2:g.93954075T= | GRCh38 |
| NC_000009.11:g.96716357T= , CM000671.1:g.96716357T= | GRCh37 |
| NC_000009.10:g.95756178T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253968.11:c.223+849A= MANE Select | ENSP00000253968.5:n.223+849A= | |
| ENST00000253968.10:c.223+849A= | ENSP00000253968.5:n.223+849A= | |
| NM_021570.3:c.223+849A= | NP_067545.3:n.223+849A= | |
| NM_021570.4:c.223+849A= MANE Select | NP_067545.3:n.223+849A= |