Linked Data
gnomAD v4:
11-18269974-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.18269974G>T , CM000673.2:g.18269974G>T | GRCh38 |
| NC_000011.9:g.18291521G>T , CM000673.1:g.18291521G>T | GRCh37 |
| NC_000011.8:g.18248097G>T | NCBI36 |
| NG_021330.1:g.8714G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356524.8:c.*119G>T | ENSP00000348918.4:n.*119G>T | |
| ENST00000405158.2:c.*119G>T | ENSP00000384906.2:n.*119G>T | |
| NM_000331.4:c.*119G>T | NP_000322.2:n.*119G>T | |
| NM_001178006.1:c.*119G>T | NP_001171477.1:n.*119G>T | |
| NM_199161.3:c.*119G>T | NP_954630.1:n.*119G>T | |
| NM_000331.5:c.*119G>T | NP_000322.2:n.*119G>T | |
| NM_001178006.2:c.*119G>T | NP_001171477.1:n.*119G>T | |
| NM_199161.4:c.*119G>T | NP_954630.1:n.*119G>T |