Linked Data
gnomAD v4:
17-41586869-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586869G>T , CM000679.2:g.41586869G>T | GRCh38 |
| NC_000017.10:g.39743121G>T , CM000679.1:g.39743121G>T | GRCh37 |
| NC_000017.9:g.36996647G>T | NCBI36 |
| NG_008624.1:g.5027C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.-35C>A MANE Select | ENSP00000167586.6:n.-35C>A | |
| ENST00000167586.6:c.-35C>A | ENSP00000167586.6:n.-35C>A | |
| NM_000526.4:c.-35C>A | NP_000517.2:n.-35C>A | |
| NM_000526.5:c.-35C>A MANE Select | NP_000517.3:n.-35C>A |