Linked Data
gnomAD v4:
13-48037695-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48037695G>T , CM000675.2:g.48037695G>T | GRCh38 |
| NC_000013.10:g.48611831G>T , CM000675.1:g.48611831G>T | GRCh37 |
| NC_000013.9:g.47509832G>T | NCBI36 |
| NG_047021.1:g.5129G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643246.1:c.-252C>A (SUCLA2) | ENSP00000496235.1:n.-252C>A | |
| ENST00000646804.1:c.-174C>A (SUCLA2) | ENSP00000493977.1:n.-174C>A | |
| ENST00000258662.2:c.-52G>T (NUDT15) | ENSP00000258662.1:n.-52G>T | |
| NM_001304745.1:c.-52G>T (NUDT15) | NP_001291674.1:n.-52G>T | |
| NM_018283.2:c.-52G>T (NUDT15) | NP_060753.1:n.-52G>T | |
| NM_018283.3:c.-52G>T (NUDT15) | NP_060753.1:n.-52G>T | |
| NR_136687.1:n.129G>T (NUDT15) | ||
| NR_136688.1:n.129G>T (NUDT15) |