Linked Data
gnomAD v4:
15-38252973-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252973G>A , CM000677.2:g.38252973G>A | GRCh38 |
| NC_000015.9:g.38545174G>A , CM000677.1:g.38545174G>A | GRCh37 |
| NC_000015.8:g.36332466G>A | NCBI36 |
| NG_008980.1:g.5123G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-213G>A MANE Select | ENSP00000299084.4:n.-213G>A | |
| ENST00000299084.8:c.-213G>A | ENSP00000299084.4:n.-213G>A | |
| ENST00000561205.1:n.126G>A | ||
| NM_152594.2:c.-213G>A | NP_689807.1:n.-213G>A | |
| XM_005254202.2:c.-213G>A | XP_005254259.1:n.-213G>A | |
| XM_005254203.3:c.-260G>A | XP_005254260.1:n.-260G>A | |
| XM_005254202.3:c.-213G>A | XP_005254259.1:n.-213G>A | |
| XR_001751484.1:n.87+594C>T | ||
| NM_152594.3:c.-213G>A MANE Select | NP_689807.1:n.-213G>A |