Linked Data
gnomAD v4:
10-94850169-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94850169T>A , CM000672.2:g.94850169T>A | GRCh38 |
| NC_000010.10:g.96609926T>A , CM000672.1:g.96609926T>A | GRCh37 |
| NC_000010.9:g.96599916T>A | NCBI36 |
| NG_008384.2:g.92464T>A | |
| NG_008384.3:g.92489T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.1291+111T>A MANE Select | ENSP00000360372.3:n.1291+111T>A | |
| ENST00000645461.1:n.2202+111T>A | ||
| ENST00000371321.7:c.1291+111T>A | ENSP00000360372.3:n.1291+111T>A | |
| ENST00000464755.1:c.2054+111T>A | ENSP00000483243.1:n.2054+111T>A | |
| NM_000769.2:c.1291+111T>A | NP_000760.1:n.1291+111T>A | |
| NM_000769.4:c.1291+111T>A MANE Select | NP_000760.1:n.1291+111T>A |