| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.181861392T= , CM000666.2:g.181861392T= | GRCh38 |
| NC_000004.11:g.182782545T= , CM000666.1:g.182782545T= | GRCh37 |
| NC_000004.10:g.183019539T= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| XM_017008385.1:c.-236-6360T= | XP_016863874.1:n.-236-6360T= |
| XM_017008389.1:c.-236-6360T= | XP_016863878.1:n.-236-6360T= |
| XM_017008390.1:c.-236-6360T= | XP_016863879.1:n.-236-6360T= |
| XM_017008391.1:c.-236-6360T= | XP_016863880.1:n.-236-6360T= |
| XM_017008392.1:c.-236-6360T= | XP_016863881.1:n.-236-6360T= |
| XM_017008393.1:c.-236-6360T= | XP_016863882.1:n.-236-6360T= |
| XM_017008394.1:c.-236-6360T= | XP_016863883.1:n.-236-6360T= |
| XR_939532.1:n.318-6360T= |