Linked Data
gnomAD v4:
11-299448-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.299448G>T , CM000673.2:g.299448G>T | GRCh38 |
| NC_000011.9:g.299448G>T , CM000673.1:g.299448G>T | GRCh37 |
| NC_000011.8:g.289448G>T | NCBI36 |
| NG_032892.1:g.5079C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382614.2:c.43C>A MANE Select | ENSP00000372059.2:p.Pro15Thr | |
| NM_001025295.2:c.43C>A | NP_001020466.1:p.Pro15Thr | |
| NM_001025295.3:c.43C>A MANE Select | NP_001020466.1:p.Pro15Thr |