Linked Data
gnomAD v4:
17-42911439-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911439C>T , CM000679.2:g.42911439C>T | GRCh38 |
| NC_000017.10:g.41063456C>T , CM000679.1:g.41063456C>T | GRCh37 |
| NC_000017.9:g.38316982C>T | NCBI36 |
| NG_011808.1:g.15642C>T , LRG_147:g.15642C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.*13C>T MANE Select | ENSP00000253801.1:n.*13C>T | |
| ENST00000253801.6:c.*13C>T | ENSP00000253801.1:n.*13C>T | |
| ENST00000585489.1:c.*479C>T | ENSP00000466202.1:n.*479C>T | |
| NM_000151.3:c.*13C>T | NP_000142.2:n.*13C>T | |
| NM_001270397.1:c.*479C>T | NP_001257326.1:n.*479C>T | |
| NM_000151.4:c.*13C>T MANE Select | NP_000142.2:n.*13C>T | |
| NM_001270397.2:c.*479C>T | NP_001257326.1:n.*479C>T |