Linked Data
ClinVar Variation Id:
521386
ClinVar RCV Id:
RCV000624521
dbSNP Id:
rs775177277
ExAC:
15:49048540 G / A
gnomAD v2:
15-49048540-G-A
gnomAD v4:
15-48756343-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48756343G>A , CM000677.2:g.48756343G>A | GRCh38 |
| NC_000015.9:g.49048540G>A , CM000677.1:g.49048540G>A | GRCh37 |
| NC_000015.8:g.46835832G>A | NCBI36 |
| NG_027518.1:g.59804C>T | |
| NG_027518.2:g.59804C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380950.7:c.2905C>T MANE Select | ENSP00000370337.2:p.His969Tyr | |
| ENST00000325747.9:c.2626C>T | ENSP00000321000.5:p.His876Tyr | |
| ENST00000380950.6:c.2905C>T | ENSP00000370337.2:p.His969Tyr | |
| ENST00000399334.7:c.2905C>T | ENSP00000382271.3:p.His969Tyr | |
| NM_001194998.1:c.2905C>T | NP_001181927.1:p.His969Tyr | |
| NM_014985.3:c.2905C>T | NP_055800.2:p.His969Tyr | |
| XM_006720437.2:c.2905C>T | XP_006720500.1:p.His969Tyr | |
| XM_011521373.1:c.2905C>T | XP_011519675.1:p.His969Tyr | |
| XM_011521374.1:c.2905C>T | XP_011519676.1:p.His969Tyr | |
| XM_011521375.1:c.2905C>T | XP_011519677.1:p.His969Tyr | |
| XM_011521376.1:c.2905C>T | XP_011519678.1:p.His969Tyr | |
| XM_011521377.1:c.2905C>T | XP_011519679.1:p.His969Tyr | |
| XM_011521378.1:c.2905C>T | XP_011519680.1:p.His969Tyr | |
| XM_011521379.1:c.2905C>T | XP_011519681.1:p.His969Tyr | |
| XM_011521380.1:c.946C>T | XP_011519682.1:p.His316Tyr | |
| XM_011521381.1:c.940C>T | XP_011519683.1:p.His314Tyr | |
| XR_931769.1:n.3870C>T | ||
| XR_931770.1:n.3870C>T | ||
| XR_931771.1:n.3870C>T | ||
| XR_931772.1:n.3870C>T | ||
| XR_931773.1:n.3870C>T | ||
| XR_931774.1:n.3870C>T | ||
| XR_931775.1:n.3870C>T | ||
| XM_006720437.3:c.2905C>T | XP_006720500.1:p.His969Tyr | |
| XM_011521373.3:c.2905C>T | XP_011519675.1:p.His969Tyr | |
| XM_011521374.3:c.2905C>T | XP_011519676.1:p.His969Tyr | |
| XM_011521375.3:c.2905C>T | XP_011519677.1:p.His969Tyr | |
| XM_011521378.3:c.2905C>T | XP_011519680.1:p.His969Tyr | |
| XM_011521379.3:c.2905C>T | XP_011519681.1:p.His969Tyr | |
| XM_011521381.2:c.940C>T | XP_011519683.1:p.His314Tyr | |
| XM_017022015.1:c.940C>T | XP_016877504.1:p.His314Tyr | |
| XM_024449875.1:c.2905C>T | XP_024305643.1:p.His969Tyr | |
| XR_001751153.2:n.3856C>T | ||
| XR_931769.3:n.3856C>T | ||
| XR_931770.3:n.3856C>T | ||
| XR_931775.3:n.3856C>T | ||
| NM_001194998.2:c.2905C>T MANE Select | NP_001181927.1:p.His969Tyr | |
| NM_014985.4:c.2905C>T | NP_055800.2:p.His969Tyr |