Linked Data
dbSNP Id:
rs373616950
ExAC:
19:34890955 T / G
gnomAD v2:
19-34890955-T-G
gnomAD v3:
19-34400050-T-G
gnomAD v4:
19-34400050-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.34400050T>G , CM000681.2:g.34400050T>G | GRCh38 |
| NC_000019.9:g.34890955T>G , CM000681.1:g.34890955T>G | GRCh37 |
| NC_000019.8:g.39582795T>G | NCBI36 |
| NG_012838.2:g.40311T>G | |
| NG_012838.3:g.45459T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356487.11:c.*14T>G MANE Select | ENSP00000348877.3:n.*14T>G | |
| ENST00000415930.8:c.*14T>G | ENSP00000405573.3:n.*14T>G | |
| ENST00000586425.2:c.1357T>G | ||
| ENST00000588991.7:c.*14T>G | ENSP00000465858.3:n.*14T>G | |
| ENST00000643067.1:n.2736T>G | ||
| ENST00000647446.1:c.*742T>G | ENSP00000495129.1:n.*742T>G | |
| ENST00000356487.9:c.*14T>G | ENSP00000348877.3:n.*14T>G | |
| ENST00000415930.7:c.*14T>G | ENSP00000405573.2:n.*14T>G | |
| ENST00000586077.1:n.2768T>G | ||
| ENST00000586392.1:n.1429T>G | ||
| ENST00000586425.1:c.*123T>G | ENSP00000467670.2:n.*123T>G | |
| ENST00000588991.6:c.1736T>G | ENSP00000465858.2:n.1736T>G | |
| ENST00000592740.5:c.193+3393T>G | ||
| NM_000175.3:c.*14T>G | NP_000166.2:n.*14T>G | |
| NM_001184722.1:c.*14T>G | NP_001171651.1:n.*14T>G | |
| NM_001289789.1:c.*14T>G | NP_001276718.1:n.*14T>G | |
| NM_001289790.1:c.*14T>G | NP_001276719.1:n.*14T>G | |
| XM_005258764.1:c.*14T>G | XP_005258821.1:n.*14T>G | |
| XM_006723148.1:c.*14T>G | XP_006723211.1:n.*14T>G | |
| XM_011526754.1:c.*14T>G | XP_011525056.1:n.*14T>G | |
| NM_000175.5:c.*14T>G MANE Select | NP_000166.2:n.*14T>G | |
| NM_001289790.2:c.*14T>G | NP_001276719.1:n.*14T>G | |
| NM_001329909.1:c.*14T>G | NP_001316838.1:n.*14T>G | |
| NM_001329910.1:c.*14T>G | NP_001316839.1:n.*14T>G | |
| NM_001329911.1:c.*14T>G | NP_001316840.1:n.*14T>G | |
| XM_011526754.3:c.*14T>G | XP_011525056.1:n.*14T>G | |
| NM_001289790.3:c.*14T>G | NP_001276719.1:n.*14T>G | |
| NM_001329911.2:c.*14T>G | NP_001316840.1:n.*14T>G |