Linked Data
gnomAD v4:
1-114705709-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114705711del , CM000663.2:g.114705711del | GRCh38 |
| NC_000001.10:g.115248332del , CM000663.1:g.115248332del | GRCh37 |
| NC_000001.9:g.115049855del | NCBI36 |
| NG_007572.1:g.16185del , LRG_92:g.16185del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*2384del MANE Select | ENSP00000358548.4:n.*2384del | |
| ENST00000369535.4:c.*2384del | ENSP00000358548.4:n.*2384del | |
| NM_002524.4:c.*2384del | NP_002515.1:n.*2384del | |
| NM_002524.5:c.*2384del MANE Select | NP_002515.1:n.*2384del |