Linked Data
gnomAD v4:
15-38253216-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38253216G>T , CM000677.2:g.38253216G>T | GRCh38 |
| NC_000015.9:g.38545417G>T , CM000677.1:g.38545417G>T | GRCh37 |
| NC_000015.8:g.36332709G>T | NCBI36 |
| NG_008980.1:g.5366G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.31G>T MANE Select | ENSP00000299084.4:p.Asp11Tyr | |
| ENST00000299084.8:c.31G>T | ENSP00000299084.4:p.Asp11Tyr | |
| ENST00000561205.1:n.369G>T | ||
| ENST00000561317.1:c.-97G>T | ENSP00000453680.1:n.-97G>T | |
| NM_152594.2:c.31G>T | NP_689807.1:p.Asp11Tyr | |
| XM_005254202.2:c.31G>T | XP_005254259.1:p.Glu11Ter | |
| XM_005254203.3:c.-17G>T | XP_005254260.1:n.-17G>T | |
| XM_005254202.3:c.31G>T | XP_005254259.1:p.Glu11Ter | |
| XR_001751484.1:n.87+351C>A | ||
| NM_152594.3:c.31G>T MANE Select | NP_689807.1:p.Asp11Tyr |