Linked Data
gnomAD v4:
15-38253201-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38253201G>A , CM000677.2:g.38253201G>A | GRCh38 |
| NC_000015.9:g.38545402G>A , CM000677.1:g.38545402G>A | GRCh37 |
| NC_000015.8:g.36332694G>A | NCBI36 |
| NG_008980.1:g.5351G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.16G>A MANE Select | ENSP00000299084.4:p.Ala6Thr | |
| ENST00000299084.8:c.16G>A | ENSP00000299084.4:p.Ala6Thr | |
| ENST00000561205.1:n.354G>A | ||
| ENST00000561317.1:c.-112G>A | ENSP00000453680.1:n.-112G>A | |
| NM_152594.2:c.16G>A | NP_689807.1:p.Ala6Thr | |
| XM_005254202.2:c.16G>A | XP_005254259.1:p.Ala6Thr | |
| XM_005254203.3:c.-32G>A | XP_005254260.1:n.-32G>A | |
| XM_005254202.3:c.16G>A | XP_005254259.1:p.Ala6Thr | |
| XR_001751484.1:n.87+366C>T | ||
| NM_152594.3:c.16G>A MANE Select | NP_689807.1:p.Ala6Thr |