gnomAD v4:
Joint Max Group AF
0.00001357 (NFE)
Exomes Max Group AF
0.00001457 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10150315C>T , CM000665.2:g.10150315C>T | GRCh38 |
| NC_000003.11:g.10191999C>T , CM000665.1:g.10191999C>T | GRCh37 |
| NC_000003.10:g.10166999C>T | NCBI36 |
| NG_008212.3:g.13681C>T , LRG_322:g.13681C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*669C>T | ENSP00000512434.1:n.*669C>T | |
| ENST00000696143.1:c.1128C>T | ENSP00000512435.1:n.1128C>T | |
| ENST00000696153.1:c.*350C>T | ENSP00000512444.1:n.*350C>T | |
| ENST00000256474.3:c.*350C>T MANE Select | ENSP00000256474.3:n.*350C>T | |
| ENST00000256474.2:c.*350C>T | ENSP00000256474.2:n.*350C>T | |
| ENST00000345392.2:c.*350C>T | ENSP00000344757.2:n.*350C>T | |
| NM_000551.3:c.*350C>T , LRG_322t1:c.*350C>T | NP_000542.1:n.*350C>T | |
| NM_198156.2:c.*350C>T | NP_937799.1:n.*350C>T | |
| NM_001354723.1:c.*546C>T | NP_001341652.1:n.*546C>T | |
| NM_000551.4:c.*350C>T MANE Select | NP_000542.1:n.*350C>T | |
| NM_001354723.2:c.*546C>T | NP_001341652.1:n.*546C>T | |
| NM_198156.3:c.*350C>T | NP_937799.1:n.*350C>T |