Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281045C= , CM000678.2:g.11281045C= | GRCh38 |
| NC_000016.9:g.11374902C= , CM000678.1:g.11374902C= | GRCh37 |
| NC_000016.8:g.11282403C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000312511.4:c.113-10G= (PRM1) MANE Select | ENSP00000310515.3:n.113-10G= | |
| ENST00000649869.1:n.152+31267C= (RMI2) | ||
| ENST00000312511.3:c.113-10G= (PRM1) | ENSP00000310515.3:n.113-10G= | |
| ENST00000572173.1:c.-515-14171C= (RMI2) | ENSP00000461206.1:n.-515-14171C= | |
| ENST00000573910.1:n.160+31267C= (RMI2) | ||
| NM_002761.2:c.113-10G= (PRM1) | NP_002752.1:n.113-10G= | |
| XR_933070.1:n.733+31267C= | ||
| XR_933070.3:n.876+31267C= | ||
| NM_002761.3:c.113-10G= (PRM1) MANE Select | NP_002752.1:n.113-10G= |