Linked Data
gnomAD v4:
15-38253000-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38253005del , CM000677.2:g.38253005del | GRCh38 |
| NC_000015.9:g.38545206del , CM000677.1:g.38545206del | GRCh37 |
| NC_000015.8:g.36332498del | NCBI36 |
| NG_008980.1:g.5155del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-181del MANE Select | ENSP00000299084.4:n.-181del | |
| ENST00000299084.8:c.-181del | ENSP00000299084.4:n.-181del | |
| ENST00000561205.1:n.158del | ||
| NM_152594.2:c.-181del | NP_689807.1:n.-181del | |
| XM_005254202.2:c.-181del | XP_005254259.1:n.-181del | |
| XM_005254203.3:c.-228del | XP_005254260.1:n.-228del | |
| XM_005254202.3:c.-181del | XP_005254259.1:n.-181del | |
| XR_001751484.1:n.87+566del | ||
| NM_152594.3:c.-181del MANE Select | NP_689807.1:n.-181del |