Linked Data
ClinVar Variation Id:
97855
dbSNP Id:
rs104895486
ExAC:
16:50750581 C / T
gnomAD v2:
16-50750581-C-T
gnomAD v3:
16-50716670-C-T
gnomAD v4:
16-50716670-C-T
COSMIC:
COSM1378213
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50716670C>T , CM000678.2:g.50716670C>T | GRCh38 |
| NC_000016.9:g.50750581C>T , CM000678.1:g.50750581C>T | GRCh37 |
| NC_000016.8:g.49308082C>T | NCBI36 |
| NG_007508.1:g.24532C>T , LRG_177:g.24532C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641284.2:c.2381+4297C>T | ENSP00000493088.1:n.2381+4297C>T | |
| ENST00000646677.2:c.*230C>T | ENSP00000496533.1:n.*230C>T | |
| ENST00000697425.1:c.292C>T | ||
| ENST00000697426.1:c.264C>T | ||
| ENST00000697427.1:c.181-3255C>T | ||
| ENST00000697428.1:n.1943C>T | ||
| ENST00000641284.1:c.2381+4297C>T | ENSP00000493088.1:n.2381+4297C>T | |
| ENST00000646677.1:c.*230C>T | ENSP00000496533.1:n.*230C>T | |
| ENST00000647318.2:c.2465C>T MANE Select | ENSP00000495993.1:p.Ala822Val | |
| ENST00000300589.6:c.2546C>T | ENSP00000300589.2:p.Ala849Val | |
| ENST00000524712.5:c.208+4269C>T | ||
| ENST00000527052.5:c.180+4297C>T | ||
| ENST00000529633.5:c.209-3255C>T | ||
| ENST00000534057.1:c.264C>T | ||
| ENST00000534067.5:c.444+4033C>T | ||
| NM_001293557.1:c.2465C>T | NP_001280486.1:p.Ala822Val | |
| NM_022162.2:c.2546C>T | NP_071445.1:p.Ala849Val | |
| XM_005256084.2:c.2465C>T | XP_005256141.1:p.Ala822Val | |
| XM_006721242.2:c.2465C>T | XP_006721305.1:p.Ala822Val | |
| XM_011523257.1:c.2042C>T | XP_011521559.1:p.Ala681Val | |
| XM_011523258.1:c.2042C>T | XP_011521560.1:p.Ala681Val | |
| XM_011523259.1:c.1880C>T | XP_011521561.1:p.Ala627Val | |
| XR_429725.2:n.2472-3255C>T | ||
| XR_429726.2:n.2471+4297C>T | ||
| XR_933387.1:n.2583C>T | ||
| XM_005256084.4:c.2465C>T | XP_005256141.1:p.Ala822Val | |
| XM_006721242.4:c.2465C>T | XP_006721305.1:p.Ala822Val | |
| XM_011523259.2:c.1880C>T | XP_011521561.1:p.Ala627Val | |
| XM_017023535.1:c.1973C>T | XP_016879024.1:p.Ala658Val | |
| XM_017023536.1:c.1880C>T | XP_016879025.1:p.Ala627Val | |
| XM_017023537.1:c.1880C>T | XP_016879026.1:p.Ala627Val | |
| XM_017023538.1:c.1880C>T | XP_016879027.1:p.Ala627Val | |
| XR_429725.3:n.2425-3255C>T | ||
| XR_429726.3:n.2424+4297C>T | ||
| XR_933387.2:n.2536C>T | ||
| NM_001293557.2:c.2465C>T | NP_001280486.1:p.Ala822Val | |
| NM_001370466.1:c.2465C>T MANE Select | NP_001357395.1:p.Ala822Val | |
| NM_022162.3:c.2546C>T | NP_071445.1:p.Ala849Val | |
| NR_163434.1:n.2677C>T |