Linked Data
gnomAD v4:
4-4862690-TCG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862691_4862692del , CM000666.2:g.4862691_4862692del | GRCh38 |
| NC_000004.11:g.4864418_4864419del , CM000666.1:g.4864418_4864419del | GRCh37 |
| NC_000004.10:g.4915319_4915320del | NCBI36 |
| NG_008121.1:g.8027_8028del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.470-10_470-9del MANE Select | ENSP00000372170.4:n.470-10_470-9del | |
| ENST00000382723.4:c.470-10_470-9del | ENSP00000372170.4:n.470-10_470-9del | |
| ENST00000468421.1:n.182-10_182-9del | ||
| NM_002448.3:c.470-10_470-9del MANE Select | NP_002439.2:n.470-10_470-9del |