Linked Data
gnomAD v4:
1-17392088-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17392088C>T , CM000663.2:g.17392088C>T | GRCh38 |
| NG_032943.1:g.24843C>T | |
| NG_032943.2:g.24843C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619609.1:c.963-26C>T MANE Select | ENSP00000483125.1:n.963-26C>T | |
| NM_207421.4:c.963-26C>T MANE Select | NP_997304.3:n.963-26C>T |