Linked Data
dbSNP Id:
rs373970727
ExAC:
17:61566084 C / T
gnomAD v2:
17-61566084-C-T
gnomAD v3:
17-63488723-C-T
gnomAD v4:
17-63488723-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63488723C>T , CM000679.2:g.63488723C>T | GRCh38 |
| NC_000017.10:g.61566084C>T , CM000679.1:g.61566084C>T | GRCh37 |
| NC_000017.9:g.58919816C>T | NCBI36 |
| NG_011648.1:g.16651C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.2381C>T MANE Select | ENSP00000290866.4:p.Ala794Val | |
| ENST00000290863.10:c.659C>T | ENSP00000290863.6:p.Ala220Val | |
| ENST00000290866.9:c.2381C>T | ENSP00000290866.4:p.Ala794Val | |
| ENST00000413513.7:c.659C>T | ENSP00000392247.3:p.Ala220Val | |
| ENST00000428043.5:c.2381C>T | ENSP00000397593.2:p.Ala794Val | |
| ENST00000577647.2:c.659C>T | ENSP00000464149.1:p.Ala220Val | |
| ENST00000578839.5:c.*451C>T | ENSP00000462110.2:n.*451C>T | |
| ENST00000579204.1:c.640C>T | ENSP00000464629.1:n.640C>T | |
| ENST00000579314.5:c.*110C>T | ENSP00000462599.1:n.*110C>T | |
| ENST00000582005.5:c.*301C>T | ENSP00000462002.1:n.*301C>T | |
| ENST00000582761.1:c.149C>T | ENSP00000462909.1:p.Ala50Val | |
| ENST00000584865.5:n.327C>T | ||
| NM_000789.3:c.2381C>T | NP_000780.1:p.Ala794Val | |
| NM_001178057.1:c.659C>T | NP_001171528.1:p.Ala220Val | |
| NM_152830.2:c.659C>T | NP_690043.1:p.Ala220Val | |
| XM_005257110.1:c.1832C>T | XP_005257167.1:p.Ala611Val | |
| XM_006721737.2:c.719C>T | XP_006721800.2:p.Ala240Val | |
| XM_006721737.3:c.719C>T | XP_006721800.2:p.Ala240Val | |
| NM_000789.4:c.2381C>T MANE Select | NP_000780.1:p.Ala794Val | |
| NM_001178057.2:c.659C>T | NP_001171528.1:p.Ala220Val | |
| NM_152830.3:c.659C>T | NP_690043.1:p.Ala220Val | |
| NM_001382700.1:c.1814C>T | NP_001369629.1:p.Ala605Val | |
| NM_001382701.1:c.1529C>T | NP_001369630.1:p.Ala510Val | |
| NM_001382702.1:c.311C>T | NP_001369631.1:p.Ala104Val | |
| NR_168483.1:n.759C>T |