Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281137C>T , CM000678.2:g.11281137C>T | GRCh38 |
| NC_000016.9:g.11374994C>T , CM000678.1:g.11374994C>T | GRCh37 |
| NC_000016.8:g.11282495C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002761.3:c.102G>A (PRM1) MANE Select | NP_002752.1:p.Arg34= |
| ENST00000312511.4:c.102G>A (PRM1) MANE Select | ENSP00000310515.3:p.Arg34= |
| NM_002761.2:c.102G>A (PRM1) | NP_002752.1:p.Arg34= |
| ENST00000312511.3:c.102G>A (PRM1) | ENSP00000310515.3:p.Arg34= |
| ENST00000572173.1:c.-515-14079C>T (RMI2) | ENSP00000461206.1:n.-515-14079C>T |
| ENST00000573910.1:n.160+31359C>T (RMI2) | |
| ENST00000649869.1:n.152+31359C>T (RMI2) | |
| XR_933070.1:n.733+31359C>T | |
| XR_933070.3:n.876+31359C>T |