Linked Data
gnomAD v4:
15-38252887-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252887A>G , CM000677.2:g.38252887A>G | GRCh38 |
| NC_000015.9:g.38545088A>G , CM000677.1:g.38545088A>G | GRCh37 |
| NC_000015.8:g.36332380A>G | NCBI36 |
| NG_008980.1:g.5037A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-299A>G MANE Select | ENSP00000299084.4:n.-299A>G | |
| ENST00000299084.8:c.-299A>G | ENSP00000299084.4:n.-299A>G | |
| ENST00000561205.1:n.40A>G | ||
| NM_152594.2:c.-299A>G | NP_689807.1:n.-299A>G | |
| XM_005254202.2:c.-299A>G | XP_005254259.1:n.-299A>G | |
| XM_005254203.3:c.-346A>G | XP_005254260.1:n.-346A>G | |
| XM_005254202.3:c.-299A>G | XP_005254259.1:n.-299A>G | |
| XR_001751484.1:n.87+680T>C | ||
| NM_152594.3:c.-299A>G MANE Select | NP_689807.1:n.-299A>G |