Linked Data
gnomAD v4:
19-9126929-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.9126930del , CM000681.2:g.9126930del | GRCh38 |
| NC_000019.9:g.9237606del , CM000681.1:g.9237606del | GRCh37 |
| NC_000019.8:g.9098606del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305444.2:c.21del MANE Select | ENSP00000302867.2:p.Asp8ThrfsTer? | |
| NM_001001958.1:c.21del MANE Select | NP_001001958.1:p.Asp8ThrfsTer? |