Linked Data
gnomAD v4:
17-41586852-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586852T>C , CM000679.2:g.41586852T>C | GRCh38 |
| NC_000017.10:g.39743104T>C , CM000679.1:g.39743104T>C | GRCh37 |
| NC_000017.9:g.36996630T>C | NCBI36 |
| NG_008624.1:g.5044A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.-18A>G MANE Select | ENSP00000167586.6:n.-18A>G | |
| ENST00000167586.6:c.-18A>G | ENSP00000167586.6:n.-18A>G | |
| NM_000526.4:c.-18A>G | NP_000517.2:n.-18A>G | |
| NM_000526.5:c.-18A>G MANE Select | NP_000517.3:n.-18A>G |