Linked Data
gnomAD v4:
19-18389014-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18389014T>G , CM000681.2:g.18389014T>G | GRCh38 |
| NC_000019.9:g.18499824T>G , CM000681.1:g.18499824T>G | GRCh37 |
| NC_000019.8:g.18360824T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252809.3:c.*79T>G MANE Select | ENSP00000252809.3:n.*79T>G | |
| NM_004864.2:c.*79T>G | NP_004855.2:n.*79T>G | |
| NM_004864.3:c.*79T>G | NP_004855.2:n.*79T>G | |
| XM_024451789.1:c.*79T>G | XP_024307557.1:n.*79T>G | |
| NM_004864.4:c.*79T>G MANE Select | NP_004855.2:n.*79T>G |