Linked Data
gnomAD v4:
17-4734392-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4734392C>T , CM000679.2:g.4734392C>T | GRCh38 |
| NC_000017.10:g.4637687C>T , CM000679.1:g.4637687C>T | GRCh37 |
| NC_000017.9:g.4584436C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293778.12:c.*111G>A MANE Select | ENSP00000293778.7:n.*111G>A | |
| ENST00000574412.6:c.*214G>A | ENSP00000459592.2:n.*214G>A | |
| ENST00000293778.10:c.*111G>A | ENSP00000293778.6:n.*111G>A | |
| ENST00000574412.5:c.*214G>A | ENSP00000459592.1:n.*214G>A | |
| ENST00000576153.5:n.667G>A | ||
| NM_022059.3:c.*111G>A | NP_071342.2:n.*111G>A | |
| NM_022059.4:c.*111G>A | NP_071342.2:n.*111G>A | |
| NM_001386809.1:c.*111G>A MANE Select | NP_001373738.1:n.*111G>A |