Linked Data
gnomAD v4:
17-41586859-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586859G>T , CM000679.2:g.41586859G>T | GRCh38 |
| NC_000017.10:g.39743111G>T , CM000679.1:g.39743111G>T | GRCh37 |
| NC_000017.9:g.36996637G>T | NCBI36 |
| NG_008624.1:g.5037C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.-25C>A MANE Select | ENSP00000167586.6:n.-25C>A | |
| ENST00000167586.6:c.-25C>A | ENSP00000167586.6:n.-25C>A | |
| NM_000526.4:c.-25C>A | NP_000517.2:n.-25C>A | |
| NM_000526.5:c.-25C>A MANE Select | NP_000517.3:n.-25C>A |