Linked Data
dbSNP Id:
rs1167600157
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281346T>A , CM000678.2:g.11281346T>A | GRCh38 |
| NC_000016.9:g.11375203T>A , CM000678.1:g.11375203T>A | GRCh37 |
| NC_000016.8:g.11282704T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649869.1:n.152+31568T>A (RMI2) | ||
| ENST00000312511.3:c.-108A>T (PRM1) | ENSP00000310515.3:n.-108A>T | |
| ENST00000572173.1:c.-515-13870T>A (RMI2) | ENSP00000461206.1:n.-515-13870T>A | |
| ENST00000573910.1:n.160+31568T>A (RMI2) | ||
| XR_933070.1:n.733+31568T>A | ||
| XR_933070.3:n.876+31568T>A |