Linked Data
gnomAD v4:
16-11281349-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11281349G>T , CM000678.2:g.11281349G>T | GRCh38 |
| NC_000016.9:g.11375206G>T , CM000678.1:g.11375206G>T | GRCh37 |
| NC_000016.8:g.11282707G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649869.1:n.152+31571G>T (RMI2) | ||
| ENST00000312511.3:c.-111C>A (PRM1) | ENSP00000310515.3:n.-111C>A | |
| ENST00000572173.1:c.-515-13867G>T (RMI2) | ENSP00000461206.1:n.-515-13867G>T | |
| ENST00000573910.1:n.160+31571G>T (RMI2) | ||
| XR_933070.1:n.733+31571G>T | ||
| XR_933070.3:n.876+31571G>T |