Linked Data
gnomAD v4:
4-4862620-CTAT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862626_4862628del , CM000666.2:g.4862626_4862628del | GRCh38 |
| NC_000004.11:g.4864353_4864355del , CM000666.1:g.4864353_4864355del | GRCh37 |
| NC_000004.10:g.4915254_4915256del | NCBI36 |
| NG_008121.1:g.7962_7964del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.470-75_470-73del MANE Select | ENSP00000372170.4:n.470-75_470-73del | |
| ENST00000382723.4:c.470-75_470-73del | ENSP00000372170.4:n.470-75_470-73del | |
| ENST00000468421.1:n.181+18_181+20del | ||
| NM_002448.3:c.470-75_470-73del MANE Select | NP_002439.2:n.470-75_470-73del |