Linked Data
gnomAD v4:
4-24800197-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800198del , CM000666.2:g.24800198del | GRCh38 |
| NC_000004.11:g.24801820del , CM000666.1:g.24801820del | GRCh37 |
| NC_000004.10:g.24410918del | NCBI36 |
| NG_012213.1:g.9736del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.677del MANE Select | ENSP00000371554.3:p.Ser226Ter | |
| ENST00000382120.3:c.677del | ENSP00000371554.3:p.Ser226Ter | |
| NM_003102.2:c.677del | NP_003093.2:p.Ser226Ter | |
| XR_427488.1:n.867del | ||
| NM_003102.3:c.677del | NP_003093.2:p.Ser226Ter | |
| NM_003102.4:c.677del MANE Select | NP_003093.2:p.Ser226Ter |