Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.64092333C>A , CM000665.2:g.64092333C>A | GRCh38 |
| NC_000003.11:g.64078009C>A , CM000665.1:g.64078009C>A | GRCh37 |
| NC_000003.10:g.64053049C>A | NCBI36 |
| NG_031930.1:g.138123G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638394.2:c.*6718G>T (PRICKLE2) MANE Select | ENSP00000492363.1:n.*6718G>T | |
| NR_045697.1:n.199-2761C>A (PRICKLE2-AS1) | ||
| NM_198859.4:c.*6718G>T (PRICKLE2) MANE Select | NP_942559.1:n.*6718G>T | |
| NM_001370528.1:c.*6718G>T (PRICKLE2) | NP_001357457.1:n.*6718G>T |