Linked Data
dbSNP Id:
rs933390771
gnomAD v2:
17-61564062-C-T
gnomAD v3:
17-63486701-C-T
gnomAD v4:
17-63486701-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63486701C>T , CM000679.2:g.63486701C>T | GRCh38 |
| NC_000017.10:g.61564062C>T , CM000679.1:g.61564062C>T | GRCh37 |
| NC_000017.9:g.58917794C>T | NCBI36 |
| NG_011648.1:g.14629C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.2203C>T MANE Select | ENSP00000290866.4:p.Gln735Ter | |
| ENST00000290863.10:c.481C>T | ENSP00000290863.6:p.Gln161Ter | |
| ENST00000290866.9:c.2203C>T | ENSP00000290866.4:p.Gln735Ter | |
| ENST00000413513.7:c.481C>T | ENSP00000392247.3:p.Gln161Ter | |
| ENST00000428043.5:c.2203C>T | ENSP00000397593.2:p.Gln735Ter | |
| ENST00000577647.2:c.481C>T | ENSP00000464149.1:p.Gln161Ter | |
| ENST00000578839.5:c.*273C>T | ENSP00000462110.2:n.*273C>T | |
| ENST00000579204.1:c.384C>T | ENSP00000464629.1:n.384C>T | |
| ENST00000579314.5:c.481C>T | ENSP00000462599.1:p.Gln161Ter | |
| ENST00000579726.5:c.765C>T | ||
| ENST00000582005.5:c.*123C>T | ENSP00000462002.1:n.*123C>T | |
| NM_000789.3:c.2203C>T | NP_000780.1:p.Gln735Ter | |
| NM_001178057.1:c.481C>T | NP_001171528.1:p.Gln161Ter | |
| NM_152830.2:c.481C>T | NP_690043.1:p.Gln161Ter | |
| XM_005257110.1:c.1654C>T | XP_005257167.1:p.Gln552Ter | |
| XM_006721737.2:c.541C>T | XP_006721800.2:p.Gln181Ter | |
| XM_006721737.3:c.541C>T | XP_006721800.2:p.Gln181Ter | |
| NM_000789.4:c.2203C>T MANE Select | NP_000780.1:p.Gln735Ter | |
| NM_001178057.2:c.481C>T | NP_001171528.1:p.Gln161Ter | |
| NM_152830.3:c.481C>T | NP_690043.1:p.Gln161Ter | |
| NM_001382700.1:c.1636C>T | NP_001369629.1:p.Gln546Ter | |
| NM_001382701.1:c.1351C>T | NP_001369630.1:p.Gln451Ter | |
| NM_001382702.1:c.133C>T | NP_001369631.1:p.Gln45Ter | |
| NR_168483.1:n.503C>T |